ChemicalBook--->CAS DataBase List--->54274-80-5

54274-80-5

54274-80-5 Structure

54274-80-5 Structure
IdentificationBack Directory
[Name]

(1r,4r)-methyl 4-formylcyclohexanecarboxylate
[CAS]

54274-80-5
[Synonyms]

Methyl 4-forMylcyclohexanecarboxylate
(E)-Methyl 4-forMylcyclohexanecarboxylate
Methyl trans-4-forMylcyclohexanecarboxylate
trans-Methyl 4-forMylcyclohexanecarboxylate
(1r,4r)-methyl 4-formylcyclohexanecarboxylate
Methyl trans-4-formylcyclohexane-1-carboxylate
methyl(1r,4r)-4-formylcyclohexane-1-carboxylate
trans-4-formyl-cyclohexanecarboxylic acid methyl ester
Cyclohexanecarboxylic acid, 4-formyl-, methyl ester,trans-
[Molecular Formula]

C9H14O3
[MDL Number]

MFCD12965033
[MOL File]

54274-80-5.mol
[Molecular Weight]

170.206
Chemical PropertiesBack Directory
[Boiling point ]

236.4±33.0 °C(Predicted)
[density ]

1.129±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

liquid
[color ]

Colourless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HS Code ]

2918300090
Spectrum DetailBack Directory
[Spectrum Detail]

(1r,4r)-methyl 4-formylcyclohexanecarboxylate(54274-80-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

(1r,4r)-methyl 4-(hydroxymethyl)cyclohexanecarboxylate

110928-44-4

(1r,4r)-methyl 4-formylcyclohexanecarboxylate

54274-80-5

The general procedure for the synthesis of trans-methyl-4-(hydroxymethyl)cyclohexanecarboxylic acid from methyl trans-4-(hydroxymethyl)cyclohexanecarboxylate was as follows: oxalyl chloride (7.74 g, 61.0 mmol) was slowly added to an anhydrous dichloromethane (400 mL) solution of dimethyl sulfoxide (9.53 g, 122 mmol) at -78 °C. After removing the cooling bath, the reaction mixture was stirred at -50 °C for 5 min. Subsequently, a solution of methyl trans-4-hydroxymethyl-cyclohexanecarboxylate (8.75 g, 50.8 mmol) in dichloromethane (108 mL) was added at -65 °C. After continued stirring for 30 minutes, triethylamine (25.7 g, 254 mmol) was added. Fifteen minutes after the addition was complete, the cooling bath was removed. The reaction mixture was quenched with 1 M aqueous hydrochloric acid (152 mL, 152 mmol) at -10 °C. The organic and aqueous layers were separated, and the organic layer was washed sequentially with two parts of 250 mL of water and one part of 100 mL of brine, and then dried with anhydrous sodium sulfate. Finally, a yellow oily trans-methyl-4-formylcyclohexanecarboxylic acid (9.3 g, quantitative yield) was obtained by vacuum concentration, which could be used directly in the next reaction without further purification.MS m/e: 170 (M+).

[References]

[1] Patent: US2014/221350, 2014, A1. Location in patent: Paragraph 0168
[2] Patent: EP1772454, 2007, A1. Location in patent: Page/Page column 55-56
[3] Patent: WO2013/192088, 2013, A1. Location in patent: Paragraph 00216
[4] ChemMedChem, 2016, vol. 11, # 1, p. 31 - 37
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