Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873635Generated: October 30, 2026

m-Chloroperbenzoic acid → 5-Bromo-2-methoxyphenol

https://huagongshe.com/reaction/873635

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Bromo-2-methoxybenzaldehydeHCID 90684—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-methoxyphenolHCID 142228369.1%

Reaction Steps

To a solution of 5-bromo-2-methoxy-benzaldehyde (8 g, 4.67 mmol) dissolved in methylene chloride (24 mL) at 0° C. is slowly added a solution of m-chloroperoxybenzoic acid (10.90 g, 5.60 mmol) in methylene chloride (80 mL). The reaction mixture is slowly warmed up to room temperature and stirred for 72 h. The white solid is filtered off and the filtrate is stirred for 2 h with 2 M sodium sulfite (32 mL). The organic layer is concentrated in vacuo then the residue is dissolved in diethyl ether and washed with 1 M sodium sulfite and a half-saturated sodium bicarbonate solution. The organic phase is extracted with 2 M sodium hydroxide. The combined basic extract is acidified to pH 3-4 with concentrated HCl, and extracted with diethyl ether. The combined organic extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo to provide 3.5 g (37%) of the title compound as a brown solid. 1H NMR (CDCl3): δ 7.10 (d, J=2 Hz, 1H), 7.00 (dd, J=8, 2 Hz, 1H), 6.70 (d, J=8 Hz, 1H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-28567837d7164e15b9d8bc19feb2d0a6
Source noteuspto-grants-2015_03