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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063862Generated: November 4, 2026

Water → 7-Bromo-5-benzofuranmethanol

https://huagongshe.com/reaction/1063862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium FluorideHCID 5235—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 22144801HCID 22144801—
SolventDichloromethaneHCID 6344—
Product7-Bromo-5-benzofuranmethanolHCID 2214491851.1%

Reaction Steps

A solution of 1.1 gm (4.31 mMol) 5-(methoxycarbonyl)-7-bromobenzofuran in 20 ml dichloromethane was cooled to −78° C. To this solution were then added 2.7 ml (15.1 mMol) diisobutylaluminum hydride. The reaction mixture was allowed to warm to room temperature and was then stirred for 10 minutes. To the reaction mixture were then added 2.5 gm sodium fluoride and 815 μL water. The resulting mixture was diluted with an additional 10 ml dichloromethane and was then stirred for about 1 hour. The suspension was filtered and the filtrate concentrated under reduced pressure to provide 0.50 gm (51%) of the desired compound. The recovered solid was partitioned between 200 ml ethyl acetate and 100 ml Rochelle's Salt solution for 2 hours. This mixture was filtered, the phases separated, and the organic phase concentrated under reduced pressure to provide an additional 0.30 gm (31%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967201B1
Source datasetuspto-grants-2005_11
ORD IDord-dd0f7b1fbab04da99e31588e8fa9e47b
Source noteuspto-grants-2005_11