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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046456Generated: November 1, 2026

Toluene → 4-Methylcyclohex-3-ene-1-carbonyl chloride

https://huagongshe.com/reaction/1046456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantOxalyl chlorideHCID 65578—
Reactant(1S)-4-methylcyclohex-3-ene-1-carboxylic acidHCID 10877190—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-Methylcyclohex-3-ene-1-carbonyl chlorideHCID 12951475—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1S)-4-Methyl-cyclohex-3-enecarboxylic acid (209 mg, 1.5 mmol), azeotropically dried by evaporation from toluene, was treated with potassium phosphate tribasic (383 mg, 1.8 mmol), suspended in dichloromethane (4 mL) and treated with dimethylformamide (2 drops). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.3 mL, 3.2 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 2 h. After filtering the solids, the solution was concentrated, treated with hexanes and concentrated again to afford 4-methyl-cyclohex-3-enecarbonyl chloride (S) as a light yellow oil which was used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569302B2
Source datasetuspto-grants-2013_10
ORD IDord-dd27bbce076d4f479e2567e220183770
Source noteuspto-grants-2013_10