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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014146Generated: October 31, 2026

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

https://huagongshe.com/reaction/1014146

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 numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-b42548469f0647ebbd3be4dd45390620
Source noteuspto-grants-2011_07