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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643668Generated: October 25, 2026

m-Chloroperbenzoic acid → 3,5-Bis-benzyloxy-4-oxiranylmethyl-benzoic acid tert-butyl ester

https://huagongshe.com/reaction/1643668

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-Allyl-3,5-bis-benzyloxy-benzoic acid tert-butyl esterHCID 59560271—
SolventDichloromethaneHCID 6344—
Product3,5-Bis-benzyloxy-4-oxiranylmethyl-benzoic acid tert-butyl esterHCID 5956023657.9%

Reaction Steps

To a solution of 4-allyl-3,5-bis-benzyloxy-benzoic acid tert-butyl ester (200d) (125 g, 0.29 mol) in CH2Cl2 was added m-CPBA (100 g, 0.58 mol) in several portions. The mixture was refluxed overnight. The solid was filtered and washed with CH2Cl2. The combined filtrates were washed with saturated aqueous Na2S2O4 (250 mL) and brine (250 mL). The organic layer was dried over Na2SO4 and concentrated to give a yellow oil. The crude oil was purified by flash column chromatography (EtOAc/petroleum ether=1/20) to give the title compound (75 g, 57.8%) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.40 (m, 12H), 5.09(s, 4H), 3.53 (dd, 1H), 3.17 (m, 1H), 2.80 (dd, H), 2.63 (t, 1H), 2.51 (dd, 1H), 1.60 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-c51190fac9d6415d97581554edfa7828
Source noteuspto-grants-2012_02