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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056750Generated: October 30, 2026

2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid → 2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanol

https://huagongshe.com/reaction/2056750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acidHCID 69307806—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanolHCID 69306515—

Reaction Conditions

Temperature0 °C

Reaction Steps

(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid (1.91 g, 9.0 mmol) was dissolved in dry THF (8 mL) under nitrogen and cooled to 0° C. Borane-dimethylsulfide complex (0.155 mL, 1.64 mmol) was added by syringe. After 1 h the cooling bath was removed and the solution was stirred at room temperature for 2 h. The solution was partitioned between saturated aqueous sodium hydrogen carbonate and diethyl ether. The aqueous layer was further extracted with ether, and the combined organic layers washed with brine, dried (MgSO4), filtered and concentrated in vacuo. This yielded the title compound as a white solid (>98% ee by chiral HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335660B2
Source datasetuspto-grants-2008_02
ORD IDord-979dfce3043c4d37a2d9a222ef4b9e10
Source noteuspto-grants-2008_02