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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266125Generated: November 4, 2026

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

https://huagongshe.com/reaction/2266125

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product2,3-Dihydro-1,4-benzodioxin-6-olHCID 911527396.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2,3-dihydro-benzo[1,4]dioxin-6-carboxaldehyde (30.0 g, 183 mmol) in 500 ml CH2Cl2 was added mCPBA (37.85 g, 219 mmol). The suspension was heated to 50° C. After 16 h saturated NaHCO3 was added and the mixture was extracted with CH2Cl2 The combined organics were concentrated in vacuo and taken up in MeOH and 200 ml 4M NaOH was added. After 2 h the mixture was acidified with 4M HCl and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, washed with brine, concentrated in vacuo, and taken up in CH2Cl2. The solution was filtered to remove the precipitate. The resulting solution was stirred with saturated NaHCO3 for 1 h, separated, dried over MgSO4, filtered and concentrated in vacuo to give 2,3-dihydro-benzo[1,4]dioxin-6-ol (26.92 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858632B2
Source datasetuspto-grants-2010_12
ORD IDord-8a8c47927abd4f32a084c47df482ab36
Source noteuspto-grants-2010_12