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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709574Generated: October 29, 2026

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

https://huagongshe.com/reaction/709574

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 numberUS09181216B2
Source datasetuspto-grants-2015_11
ORD IDord-9cd1f9f99aed42e9a35f0574ec3a16d0
Source noteuspto-grants-2015_11