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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452308Generated: October 31, 2026

4-Methylbenzoyl Chloride → Methyl 2-(4-methylbenzoyloxy)3-propionylbenzoate

https://huagongshe.com/reaction/1452308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantMethyl 2-hydroxy-3-propionylbenzoateHCID 10899812—
ProductMethyl 2-(4-methylbenzoyloxy)3-propionylbenzoateHCID 19972606—

Reaction Steps

This compound was prepared in three steps according to the methods described for Intermediate XC (first step) and Intermediate LXXX (second and third steps). In the first step, 4-methylbenzoyl chloride was used instead of 2-furanecarbonyl chloride and methyl 2-hydroxy-3-propionylbenzoate was used instead of ethyl 2-hydroxy-3-propionylbenzoate. The reaction lasted 4 hours at room temperature, yielding methyl 2-(4-methylbenzoyloxy)3-propionylbenzoate. This compound was used without purification by column chromatography for the second step, that lasted 1.5 hours at 100° C. In the third step, 96% sulfuric acid was used instead of 37% hydrochloric acid. The title compound melted at 174°-175° C. after crystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605896
Source datasetuspto-grants-1997_02
ORD IDord-adcc1a91b6424da3851641b18d9791a0
Source noteuspto-grants-1997_02