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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267409Generated: October 29, 2026

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

https://huagongshe.com/reaction/2267409

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 numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-e0f25623a509484fbbffbcb311789907
Source noteuspto-grants-2010_12