3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Product Name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- CAS No.
- 74684-38-1
- Chemical Name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Synonyms
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde;2-(3-(tert-butyl)-5-formylphenyl)-2-methylpropanenitrile
- CBNumber
- CB8144878
- Molecular Formula
- C16H24O2
- Formula Weight
- 248.36
- MOL File
- 74684-38-1.mol
3,5-Di-tert-butyl-4-methoxybenzaldehyde Property
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
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
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- HCH0044527
- Product name
- 4-(2,4-DICHLOROPHENYL)BUTANOIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.08
- Updated
- 2021/12/16
- Product number
- CD12037047
- Product name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Purity
- 97%
- Packaging
- 5g
- Price
- $594
- Updated
- 2021/12/16
- Product number
- 74684381
- Product name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Packaging
- 5g
- Price
- $624
- Updated
- 2021/12/16
- Product number
- A276336
- Product name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Purity
- 97%
- Packaging
- 25g
- Price
- $914
- Updated
- 2021/12/16
- Product number
- 74684381
- Product name
- 3,5-Di-tert-butyl-4-methoxybenzaldehyde
- Packaging
- 10g
- Price
- $940.8
- Updated
- 2021/12/16
3,5-Di-tert-butyl-4-methoxybenzaldehyde Chemical Properties,Usage,Production
Synthesis
74-88-4
1620-98-0
74684-38-1
General procedure for the synthesis of 3,5-di-tert-butyl-4-hydroxybenzaldehyde from 3,5-di-tert-butyl-4-methoxybenzaldehyde and iodomethane: (1) Sodium hydride (NaH, 1.27 g, 53 mmol) was slowly added to a solution of 3,5-di-tert-butyl-4-hydroxybenzaldehyde (5 g, 21 mmol) dissolved in anhydrous tetrahydrofuran (THF, 22.5 ml) under the protection of nitrogen gas, keeping the reaction temperature at 0 °C. After the reaction mixture was removed from the cooling bath, stirring was continued for 30 minutes. (2) Subsequently, methyl iodide (CH3I, 5.2 ml, 84 mmol) dissolved in anhydrous THF (9 ml) was added to the reaction mixture and the mixture was refluxed for 12 hours. (3) After completion of the reaction, the reaction was quenched with methanol (MeOH) and then extracted with dichloromethane (CH2Cl2). (4) The organic layers were combined, concentrated and purified by column chromatography using ethyl acetate: hexane = 1:7 as eluent. (5) The final yellow liquid product 3,5-di-tert-butyl-4-methoxybenzaldehyde (4.5 g, 87% yield) was obtained. 1H NMR (CDCl3,400MHz) δ 9.91 (s, 1H), 7.79 (s, 2H), 3.73 (s, 3H), 1.46 (s, 18H).
References
[1] Patent: US9691555, 2017, B2. Location in patent: Page/Page column 29
[2] Bioorganic and Medicinal Chemistry, 2002, vol. 10, # 10, p. 3257 - 3265
[3] New Journal of Chemistry, 2006, vol. 30, # 4, p. 583 - 591
3,5-Di-tert-butyl-4-methoxybenzaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
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