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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107552Generated: October 30, 2026

1,1-Dibromoethane → 2,3-Dihydro-1,4-benzodioxine-5-carbaldehyde

https://huagongshe.com/reaction/1107552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantSodium HydroxideHCID 14798—
Reactant2,3-DihydroxybenzaldehydeHCID 90579—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product2,3-Dihydro-1,4-benzodioxine-5-carbaldehydeHCID 279503370%

Reaction Steps

2,3-Dihydroxybenzaldehyde (58 g, 420 mmol) was added to a refluxing mixture of dibromoethane (107.4 g, 570 mmol), sodium hydroxide (35.7 g, 890 mmol) and tetrabutyl ammonium bromide (3 g) in water (50 mL). After heating at reflux for 4 h, the mixture was cooled and the organic layer separated, washed with base, dried over sodium sulfate and concentrated in vacuo. The residue was Kugelrohr distilled at 135° to give the product (48 g, 70%) which solidified on standing (mp 61-62° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060506
Source datasetuspto-grants-2000_05
ORD IDord-75172d31cca94ca4a50716e2551e37bb
Source noteuspto-grants-2000_05