ChemicalBook > CAS DataBase List > 2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE

2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE

Product Name
2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE
CAS No.
1194-16-7
Chemical Name
2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE
Synonyms
Ec-000.1609;AKOS NCG-0015;2,2-diMethyloxan-4-one;2,2-DiMethyltetrahydro-4-pyrone;2,2-dimethyl-4-tetrahydropyranone;2,2-DiMethyl-4-oxotetrahydropyran;2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-ONE;2,2-dimethyltetrahydro-4H-pyran-4-one;2,2-diMethyldihydro-2H-pyran-4(3H)-one;2,2-Dimethyltetrahydropyran-4-one ,95%
CBNumber
CB6501594
Molecular Formula
C7H12O2
Formula Weight
128.17
MOL File
1194-16-7.mol
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2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE Property

Boiling point:
60-64°C/8mm
Density 
0.964 g/cm3(Temp: 25 °C)
Flash point:
60-64°C/8mm
storage temp. 
2-8°C
Appearance
Colorless to light yellow Liquid
Water Solubility 
Slightly soluble in water.
InChI
InChI=1S/C7H12O2/c1-7(2)5-6(8)3-4-9-7/h3-5H2,1-2H3
InChIKey
BWMNOXJVRHGUQM-UHFFFAOYSA-N
SMILES
C1(C)(C)OCCC(=O)C1
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Safety

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2932990090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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N-Bromosuccinimide Price

TRC
Product number
D480893
Product name
2,2-Dimethyltetrahydropyran-4-one
Packaging
100mg
Price
$75
Updated
2021/12/16
Matrix Scientific
Product number
021441
Product name
2,2-Dimethyltetrahydropyran-4-one
Purity
95%
Packaging
250mg
Price
$21
Updated
2021/12/16
Ark Pharm
Product number
P000124490
Product name
2,2-Dimethyltetrahydropyran-4-one
Purity
95%
Packaging
250mg
Price
$27
Updated
2021/12/16
Ark Pharm
Product number
P000124490
Product name
2,2-Dimethyltetrahydropyran-4-one
Purity
95%
Packaging
1g
Price
$36
Updated
2021/12/16
Matrix Scientific
Product number
021441
Product name
2,2-Dimethyltetrahydropyran-4-one
Purity
95%
Packaging
500mg
Price
$38
Updated
2021/12/16
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2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE Chemical Properties,Usage,Production

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.

Synthesis

690-94-8

1194-16-7

The general procedure for the synthesis of 2,2-dimethyltetrahydropyran-4-one from dimethyl(vinyl)ethynylmethanol was as follows: diethyl vinyl ethynylmethanol (230 g) was slowly added to a solution containing LA g aqueous solution and SULTUNC acid (5%, 0.6 mL), the reaction was maintained under vigorous stirring for 1 h, and the temperature was slowly elevated to 85 °C. The reaction was carried out in the following manner. Sulfate (18 g) was added in batches over 4 hours at 85 °C. Upon completion of the reaction, the upper liquid layer was separated and the lower layer was neutralized with potassium carbonate and subsequently extracted twice with ether. The separated upper liquid was combined with the ether extract, washed sequentially with potassium carbonate solution and water, and dried with magnesium sulfate. After evaporation to remove the ether, the residue was subjected to vacuum distillation and the 168-175 °C fraction was collected to give the target product 2,2-dimethyltetrahydropyran-4-one (140 g, 53% yield). Anhydrous toluene (150 mL) and sodium (11 g) were heated to reflux, stirred and cooled to room temperature. To this system was slowly added a solution (5-6 mL) of ethyl chloroacetate (63 g, 0.5 mol) and 2,2-dimethyltetrahydropyran-4-one (64 g, 0.5 mol) prepared above. The remaining solution was added dropwise at 23°C over 3-4 hours. When the sodium was completely consumed, anhydrous methanol (8 mL) was added. The reaction mixture was quenched by careful pouring into ice water (100 mL), ether was added and the upper organic phase was separated. The aqueous layer was extracted with ether, all ether extracts were combined, washed with water and dried with magnesium sulfate. After evaporation of the solvent, the residue was subjected to vacuum distillation (101 °C, 2 mmHg) to give the intermediate product (74 g, 70% yield). Ethyl 5,5-dimethyl-1,6-dioxapropane-2,5-octane-2-carbonate (214 g, 1 mol) was added to an aqueous solution (30 mL) of sodium hydroxide (40 g, 1 mol) and stirred at 30 °C for 30 min. After continued stirring for 2 hours, water (200 mL) was added to dissolve the precipitate. The resulting aqueous solution of sodium 5,5-dimethyl-1,6-dioxane-2,5-octane-2-carbonate was heated to 90 °C and 15-20% hydrochloric acid (1 mol) was added dropwise at this temperature over 4 hours. The aldehyde generated during the process was distilled, the reaction solution was saturated with NaCl and extracted with ether (3 x 200 mL). The organic extracts were combined, dried with anhydrous magnesium sulfate and concentrated under vacuum. The residue was distilled under vacuum (61 °C, 7 mmHg) to give the aldehyde intermediate (80 g, 55% yield). To the cooled 2,2-dimethyl-4-formyltetrahydropyran (17 g, 0.5 mol) was added a solution of potassium permanganate (79 g, 0.5 mol) in water (1 L), keeping the reaction temperature at 25°C. After 6 hours of reaction, the MnO2 was removed by filtration and washed with water. The filtrates were combined and evaporated to a volume of 175 mL, acidified with HCl and extracted with ether. The organic phase was dried with anhydrous magnesium sulfate and concentrated under vacuum. The residue was distilled under vacuum (123 °C, 5 mmHg) to give the target carboxylic acid (71 g, 90% yield). The product of Example 82 was prepared by combining tert-butyl 3-tert-butyl-1-OXA-8-azaspiro[4.5]decane-8-carboxylate with the carboxylic acid according to the method of Examples 78 and 71 in U.S. Patent 6,489,354 and the steps of Example 11. Mass spectrometry analysis showed m/e = 585 (M + 1).

References

[1] Patent: WO2004/58763, 2004, A1. Location in patent: Page 58-59
[2] Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1940, p. 223
[3] Chem.Abstr., 1942, p. 748
[4] Chem. Zentralbl., 1942, vol. 113, # I, p. 740
[5] Zhurnal Obshchei Khimii, 1948, vol. 18, p. 1336

2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE Preparation Products And Raw materials

Raw materials

Preparation Products

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2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE Suppliers

Accela ChemBio Inc.
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View Lastest Price from 2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
2,2-Dimethyltetrahydropyran-4-one 1194-16-7
Price
US $1.60-6.60/kg
Min. Order
1kg
Purity
99%
Supply Ability
100kg
Release date
2025-06-19
Shaanxi Dideu New Materials Co. Ltd
Product
2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE 1194-16-7
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000KGS
Release date
2025-03-10
Wuhan Boyuan Import & Export Co., LTD
Product
2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE 1194-16-7
Price
US $25.00/g
Min. Order
1g
Purity
99.96%
Supply Ability
500ton
Release date
2023-06-13

1194-16-7, 2,2-DIMETHYLTETRAHYDROPYRAN-4-ONERelated Search:


  • AKOS NCG-0015
  • Tetrahydro-2,2-dimethyl-4H-pyran-4-one, 95%
  • 2,2-dimethyltetrahydro-4H-pyran-4-one
  • Ec-000.1609
  • 2,2-Dimethyltetrahydropyran-4-one ,95%
  • 2,2-diMethyldihydro-2H-pyran-4(3H)-one
  • 2,2-DiMethyltetrahydro-4-pyrone
  • 4H-Pyran-4-one, tetrahydro-2,2-diMethyl-
  • 2,2-diMethyloxan-4-one
  • 2,2-DiMethyl-4-oxotetrahydropyran
  • 2,2-dimethyl-4-tetrahydropyranone
  • 2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-ONE
  • 2,2-DIMETHYLTETRAHYDROPYRAN-4-ONE ISO 9001:2015 REACH
  • 1194-16-7