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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456299Generated: November 1, 2026

Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde

https://huagongshe.com/reaction/1456299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDihydrobenzofuranHCID 10329—
ReactantBis(1,3-dichloroisopropyl ether)HCID 93323—
ReactantSodium BicarbonateHCID 516892—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product2,3-Dihydrobenzofuran-5-carboxaldehydeHCID 735901—

Reaction Steps

A solution of 9.4 ml (83.4 mmole) 2,3-dihydrobenzofuran in 250 ml methylene dichloride was cooled under nitrogen to 0° to -5° C. and 18 ml (167 mmole)titanium tetrachloride was added dropwise at 0° C. The resulting brown mixture was stirred 10 minutes and 8.3 ml (91.6 mmole) 1,1-dichloromethyl methylether was then added dropwise at 0° C. During this addition the reaction mixture became dark red. The mixture was allowed to warm to room temperature, stirred for two hours and poured slowly into a 2 liter beaker containing 700 ml saturated aqueous sodium bicarbonate solution. The resulting mixture was filtered through diatomaceous earth and the solids washed with methylene dichloride. The separated organic layer was dried (Na2SO4) and the solvent evaporated to afford a residual oil, log (81%) of which appeared homogeneous on silica gel TLC, eluting with an ethyl acetate/hexane/5% acetic acid 1:5:5 by volume. Mass spectrum (m/e): 148 (M+), 147, 119.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843970
Source datasetuspto-grants-1998_12
ORD IDord-29e89336c8b14926a68807c194322af3
Source noteuspto-grants-1998_12