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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387656Generated: October 29, 2026

m-Chloroperbenzoic acid → 2-Chloro-3-methoxyphenol

https://huagongshe.com/reaction/2387656

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Chloro-3-methoxybenzaldehydeHCID 12575695—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3-methoxyphenolHCID 1558147170%

Reaction Steps

3-Chloroperoxybenzoic acid (760 mg, 4.396 mmol) was added portionwise to a solution of 2-Chloro-3-Methoxybenzaldehyde (500 mg, 2.931 mmol) in dichloromethane (12 ml) and the mixture was stirred for 3 hours at room temperature. Further 3-chloroperoxybenzoic acid (760 mg, 4.396 mmol) was added and mixture allowed to stir for 18 hrs. The solution was diluted with 12 ml dichloromethane and washed with saturated sodium sulphite solution (15 ml) and saturated sodium hydrogen carbonate solution (15 ml). The organic layer was dried over sodium sulphate and concentrated in vacuo to a yellow gum. The residue was dissolved in methanol (12 ml), triethylamine (0.05 ml) was added and the mixture stirred for 18 hours at room temperature. The solution was concentrated in vacuo, dissolved in diethyl ether (20 ml) and extracted with 1N sodium hydroxide (20 ml). The aqueous layer was acidified to pH1 by dropwise addition of 2N hydrochloric acid and extracted with diethyl ether (2×25 ml). These combined organic layers were dried over sodium sulphate and concentrated in vacuo to afford the title compound as a brown gum in 70% yield, 325 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268881B2
Source datasetuspto-grants-2012_09
ORD IDord-bd966616fb3c4c1b9688cb4b6e4a2a1b
Source noteuspto-grants-2012_09