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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577352Generated: October 28, 2026

m-Chloroperbenzoic acid → 2,3-Dihydro-1,4-benzodioxin-6-ol

https://huagongshe.com/reaction/577352

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
SolventDichloromethaneHCID 6344—
Product2,3-Dihydro-1,4-benzodioxin-6-olHCID 911527363.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 2,3-dihydrobenzo[b][1,4]dioxine-6-carbaldehyde (1 g, 6.09 mmol) in CH2Cl2 (16 mL) was added m-CPBA (4.204 g, 24.36 mmol). The suspension was heated at 50° C. for 2 days, was cooled to rt, was quenched with saturated NaHCO3 soln. and was extracted with CH2Cl2 (3×10 mL). The combined extract was concentrated under reduced pressure, and then was dissolved in MeOH containing NaOH. The solution was stirred at rt for 2 h, was acidified with HCl and was extracted with ethyl acetate (3×10 mL). The combined extract was washed with saturated NaHCO3 solution and brine, was dried over anhydrous Na2SO4, was filtered and was concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and was filtered. The DCM solution was dried over anhydrous Na2SO4, was filtered and was concentrated under reduced pressure to give 2,3-dihydrobenzo[b][1,4]dioxin-6-ol (0.591 g, 63%) as a reddish brown oily liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040541B2
Source datasetuspto-grants-2015_05
ORD IDord-ea7874376d6d4054b0ba742c40a04efa
Source noteuspto-grants-2015_05