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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690462Generated: November 1, 2026

Borane → (3-Chloro-1-benzothien-2-yl)methanol

https://huagongshe.com/reaction/1690462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant3-Chloro-1-benzothiophene-2-carboxylic acidHCID 307964—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloro-1-benzothien-2-yl)methanolHCID 821965—

Reaction Steps

To a solution of 3-chloro-benzo[b]thiophene-2-carboxylic acid (3.5 g, 16.6 mmol) in THF (40 mL) at 0° C. was added drop-wise 1 M borane in THF (33 mL, 33.2 mmol) via a dropping funnel. The mixture was stirred at r.t overnight. The reaction was quenched with drop-wise addition of water (6 mL). Solvent was evaporated in vacuo and the residue was partitioned between sat. sodium carbonate and ethyl acetate. The aqueous phase was extracted with ethyl acetate (100 mL), the combined organic phases was washed with water (3×100 mL), dried and concentrated to give (3-chloro-benzo[b]thiophen-2-yl)-methanol as a light yellow solid (3.4 g, 103% crude yield); 1H NMR (DMSO-d6) δ 4.8 (d, J=5.8 Hz, 2H, CH2OH), 5.87 (t, J=5.8 Hz, 1H, CH2OH), 7.42-8.04 (m, 4H, Ar). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153659B2
Source datasetuspto-grants-2012_04
ORD IDord-ab839398eceb4c07b67ed0a6fd9a2a8a
Source noteuspto-grants-2012_04