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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane | HCID 6331 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 209796-22-5 | HCID 57428854 | — |
| Product | 2-(2-Bromothiophen-3-yl)ethan-1-amine | HCID 53407299 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858785B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-e0f25623a509484fbbffbcb311789907 |
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| Source note | uspto-grants-2010_12 |
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