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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854308Generated: October 25, 2026

Oxalyl chloride → 2-Methylcyclohexanecarbonyl chloride

https://huagongshe.com/reaction/1854308

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 mixture was stirred at ambient temperature for about 4 h before it was concentrated under reduced pressure to 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 numberUS08962629B2
Source datasetuspto-grants-2015_02
ORD IDord-0c77b4dd7df1447bad3b7e84da5d64b7
Source noteuspto-grants-2015_02