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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188008Generated: November 1, 2026

Acetyl chloride → Methyl 3-hydroxy-2-methylbenzoate

https://huagongshe.com/reaction/2188008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Hydroxy-2-methylbenzoic AcidHCID 252023—
SolventMethanolHCID 887—
ProductMethyl 3-hydroxy-2-methylbenzoateHCID 1248887987.3%

Reaction Steps

Acetyl chloride (5.4 ml, 5.96 g, 76 mmol) was added dropwise to methanol (15 ml) at 0° C. in a sealed 50 ml round-bottom flask. This solution was allowed to warm to room temperature for 1 hour while stirring. To this solution 3-hydroxy-2-methyl-benzoic acid (519 mg, 3.4 mmol) was added and the solution was stirred at room temperature for 42 hours. The reaction was quenched with saturated aqueous sodium bicarbonate and solid sodium bicarbonate. The volatiles were removed in vacuo and the basic aqueous solution was then extracted with dichloromethane (4×40 ml). The combined organic extracts were dried (MgSO4), filtered, and the solvent evaporated in vacuo affording 493 mg (87%) of 3-hydroxy-2-methyl-benzoic acid methyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410556B1
Source datasetuspto-grants-2002_06
ORD IDord-f5349e10e8de4f9182c8a77c634ae1c3
Source noteuspto-grants-2002_06