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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056721Generated: October 30, 2026

Borane → 2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol

https://huagongshe.com/reaction/2056721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
ReactantSodium CarbonateHCID 10340—
Reactant2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acidHCID 10635799—
SolventTetrahydrofuranHCID 8028—
Product2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanolHCID 53687843—

Reaction Steps

To a solution of 2-((1S)-6-bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acid (21.3 g, 78.6 mmol) in anhydrous THF (65 mL) under an atmosphere of nitrogen and cooled to 0° C., was added dropwise borane.THF complex in THF (1M) (94 mL, 94 mmol). After stirring for 1 h between 0 and 10° C., the reaction mixture was treated with aqueous sodium carbonate then extracted into toluene. The organic layer was washed with dilute aqueous hydrochloric acid, then concentrated in vacuo to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335660B2
Source datasetuspto-grants-2008_02
ORD IDord-c2052c3b95db415d840ea13208e9a876
Source noteuspto-grants-2008_02