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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632555Generated: October 29, 2026

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

https://huagongshe.com/reaction/632555

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 numberUS09321753B2
Source datasetuspto-grants-2016_04
ORD IDord-da5a45d537f74724b9571127e03430d5
Source noteuspto-grants-2016_04