Basic information Safety Supplier Related

Ethyl 2,2-dimethylphenylacetate

Basic information Safety Supplier Related

Ethyl 2,2-dimethylphenylacetate Basic information

Product Name:
Ethyl 2,2-dimethylphenylacetate
Synonyms:
  • ETHYL DIMETHYLBENZENEACETATE
  • ETHYL 2,2-DIMETHYLPHENYLACETATE
  • a,a-Dimethyl-benzeneacetic Acid Ethyl Ester
  • a-methyl-hydratropic Acid Ethyl Ester
  • Ethyl 2-phenylisobutyrate
  • Ethyl a,a-Dimethylbenzeneacetate
  • Ethyl a,a-Dimethylphenylacetate
  • Ethyl Dimethylphenylacetate
CAS:
2901-13-5
MF:
C12H16O2
MW:
192.25
EINECS:
608-307-7
Product Categories:
  • Aromatics Compounds
  • Aromatics
Mol File:
2901-13-5.mol
More
Less

Ethyl 2,2-dimethylphenylacetate Chemical Properties

Boiling point:
68-71 °C(Press: 0.5-0.6 Torr)
Density 
1.0039 g/cm3
vapor pressure 
10-1013.3hPa at 96.5-234.3℃
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Oil
color 
Clear Colourless to Pale Yellow
LogP
3.5
Surface tension
5.92mN/m at 159.4mg/L and 20℃
CAS DataBase Reference
2901-13-5(CAS DataBase Reference)
More
Less

Safety Information

HS Code 
2916399090
More
Less

Ethyl 2,2-dimethylphenylacetate Usage And Synthesis

Chemical Properties

Pale Yellow Liquid

Uses

Ethyl Dimethylphenylacetate (cas# 2901-13-5) is a compound useful in organic synthesis.

Synthesis

64-17-5

826-55-1

2901-13-5

Example 1: Synthesis of ethyl 2,2-dimethylphenylacetate In a 10L three-necked flask, 2-methyl-2-phenylpropanecarboxylic acid (500g, 3.1 mol) and 2.5L of dichloromethane were added and dissolved with stirring at room temperature. Subsequently, thionyl chloride (750 g, 6.3 mol) was added slowly, and after addition, the reaction system was heated to reflux and maintained for 15 hours. After the reaction was completed, cooled to room temperature, 400mL of anhydrous ethanol was added slowly dropwise, and stirring was continued for 2 hours after the dropwise addition. The reaction solution was adjusted to pH 9-10 with 10% NaOH solution and the completion of the reaction was monitored by thin layer chromatography (TLC). The organic layer was separated, washed twice each with saturated sodium bicarbonate solution and saturated sodium chloride solution in turn, and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give a colorless oily product, ethyl 2,2-dimethylbenzeneacetate 560 g, 96% yield.

References

[1] Patent: CN104276952, 2016, B. Location in patent: Paragraph 0027; 0028
[2] MedChemComm, 2013, vol. 4, # 2, p. 367 - 370
[3] Tetrahedron, 2009, vol. 65, # 2, p. 456 - 460
[4] Journal of the American Chemical Society, 1968, vol. 90, p. 2082 - 2096
[5] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2001, vol. 40, # 8, p. 717 - 718

Ethyl 2,2-dimethylphenylacetateSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Email
sales@jingyan-chemical.com
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com