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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915167Generated: November 2, 2026

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

https://huagongshe.com/reaction/1915167

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 1M 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 numberUS08614328B2
Source datasetuspto-grants-2013_12
ORD IDord-80dfa934d87747d68ceeb3e86a9180f6
Source noteuspto-grants-2013_12