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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419492Generated: November 2, 2026

Anisole → HCID 53953369, compound

https://huagongshe.com/reaction/1419492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
Reactant2-Chloro-3-methylbenzoyl chlorideHCID 19367940—
SolventDichloromethaneHCID 6344—
ProductHCID 53953369HCID 5395336997%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-chloro-3-methylbenzoyl chloride (18.05 mmol), [prepared as described above] in dry CH2Cl2 (60 ml) was cooled to 0° C. and AICl3 (2.41 g, 1 eq.) was added. After ten minutes, anisole (1.96 ml, 1 eq.) was added. The resulting orange colored reaction mixture was allowed to warm to room temperature, stirred for 3 h and then poured on ice. The product was extracted into ether, washed with brine, and dried over MgSO4 . The solvent was evaporated in vacuo to give 3-(4-methoxybenzoyl)-2-chlorotoluene (4.55 g, 97% yield) as a solid, mp 64.7°-65.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886178
Source datasetuspto-grants-1999_03
ORD IDord-a1b2805c9a9443f9b71e39b049c4ad63
Source noteuspto-grants-1999_03