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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053488Generated: November 3, 2026

Toluene → (R)-4-methylcyclohex-3-enecarbonyl chloride

https://huagongshe.com/reaction/1053488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantOxalyl chlorideHCID 65578—
Reactant(R)-4-methylcyclohex-3-enecarboxylic acidHCID 11040781—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(R)-4-methylcyclohex-3-enecarbonyl chlorideHCID 58113947—

Reaction Conditions

Temperature0 °C

Reaction Steps

(R)-4-methylcyclohex-3-enecarboxylic acid 503 (371 mg, 2.65 mmol), azeotropically dried by evaporation from toluene, was treated with potassium phosphate tribasic (1.13 g, 7.94 mmol), suspended in dichloromethane (7.6 mL) and treated with dimethylformamide (4 drops). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.75 mL, 7.9 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 2 hours. After filtering the solids, the solution was concentrated, treated with hexanes and concentrated again to afford (R)-4-methylcyclohex-3-enecarbonyl chloride 504 as a light yellow oil which was used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393256B2
Source datasetuspto-grants-2016_07
ORD IDord-ac7c92ad7b6e41b597e8c17143a86c37
Source noteuspto-grants-2016_07