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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507633Generated: November 2, 2026

Borane → 2-(2-Bromothiophen-3-yl)ethan-1-amine

https://huagongshe.com/reaction/507633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
ReactantTetrahydrofuranHCID 8028—
Reactant209796-22-5HCID 57428854—
Product2-(2-Bromothiophen-3-yl)ethan-1-amineHCID 5340729992%

Reaction Steps

2-(2-Bromothiophen-3-yl)acetonitrile (1.44 g, 7.13 mmol) was added slowly to a stirred solution of borane in THF (1.0 M, 15.7 mL, 15.7 mmol). The mixture was then heated to reflux for 14 h. The reaction mixture was allowed to cool to ambient temperature before residual borane was destroyed by careful dropwise addition of MeOH (10 mL). After the quench was complete, HCl gas was bubbled through the solution for 20 min and then the solvent was removed in vacuo. The residue was dissolved again in MeOH (20 mL) and concentrated twice more. The resulting white solid was dissolved in a biphasic mixture of dichloromethane and 1 N aqueous NaOH. The organic layer was separated, washed with brine, dried and concentrated to a colorless oil (1.34 g, 6.50 mmol, 92% yield). MS (M+H)+ 206/208.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-42122bcf9be542a1aad524e96b3b6e63
Source noteuspto-grants-2010_08