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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506526Generated: October 30, 2026

Acetic Acid → Methyl 4-cyclohexyl-3-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/1506526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl EtherHCID 3283—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-Cyclohexyl-3-(trifluoromethyl)benzoic acidHCID 57430033—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-cyclohexyl-3-(trifluoromethyl)benzoateHCID 6716931995%

Reaction Steps

To a stirred solution of 4-cyclohexyl-3-(trifluoromethyl)benzoic acid (Preparation 118B, 0.5 g, 1.836 mmol) in dichloromethane (2 mL) and MeOH (2 mL) was added 2M diethyl ether solution of TMS-diazomethane (1.836 mL, 3.67 mmol) dropwise at 0° C. till no gas evolved. The mixture was stirred at room temperature for 1 hr before AcOH (0.210 mL, 3.67 mmol) was added at 0° C. to quench the reaction. The mixture was concentrated. To the residue was added saturated aqueous sodium bicarbonate solution (5 mL) and extracted with dichloromethane (3×3 mL). The combined dichloromethane extracts were dried (sodium sulfate) and concentrated under reduced pressure to give a liquid. Flash chromatography purification (silica gel column, 10→40% dichloromethane in n-heptane) afforded methyl 4-cyclohexyl-3-(trifluoromethyl)benzoate (0.5 g, 1.746 mmol, 95% yield) as a colorless liquid. The compound had an HPLC retention time=4.03 min. (condition C); LC/MS M+1=287.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-76260d5dd3a94c9fba19b7c7e054e898
Source noteuspto-grants-2015_12