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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204507Generated: November 2, 2026

Oxalyl chloride → 2-Methylcyclohexanecarbonyl chloride

https://huagongshe.com/reaction/2204507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methylcyclohexanecarboxylic acidHCID 85811—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Methylcyclohexanecarbonyl chlorideHCID 2759837102.3%

Reaction Steps

To a solution of 2-methylcyclohexanecarboxylic acid (6.00 mL, 42.6 mmol, mixture of cis and trans) in DCM (60 mL) was added oxalyl chloride (4.80 mL, 55.3 mmol) followed by DMF (0.03 mL, 0.4 mmol). The reaction was stirred at ambient temperature for about 4 h before it was concentrated under reduced pressure to a constant weight to afford 2-methylcyclohexanecarbonyl chloride (mixture of diastereomers) as a yellow oil (7.0 g, 97%): 1H NMR (400 MHz, CDCl3) δ 2.98-2.94 (m, 1H), 2.39-2.35 (m, 1H), 1.91-1.82 (m, 1H), 1.79-1.72 (m, 1H), 1.69-1.60 (m, 2H), 1.57-1.47 (m, 2H), 1.42-1.36 (m, 1H), 1.34-1.26 (m, 1H), 1.04-0.96 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365579B2
Source datasetuspto-grants-2016_06
ORD IDord-a8ed75cc32b14a9182ab166686ace493
Source noteuspto-grants-2016_06