HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913863Generated: October 27, 2026
Hydrochloric Acid → 3-Amino-1-(2-chloro-phenyl)-propan-1-ol hydrochloride
https://huagongshe.com/reaction/1913863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 3-(2-Chlorophenyl)-3-hydroxypropanenitrile | HCID 11975498 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Amino-1-(2-chloro-phenyl)-propan-1-ol hydrochloride | HCID 86762186 | 176.1% |
Reaction Steps
3-(2-Chloro-phenyl)-3-hydroxy-propionitrile (740 mg, 4.07 mmol) was slowly treated with a solution of borane-tetrahydrofuran complex (9 mL, 8.96 mmol, 1M in tetrahydrofuran) at 0° C. After bubbling ceased, the reaction mixture was heated to 75° C. for 2 hours and 1.1 eq of additional borane was added to drive the reaction to completion. The reaction mixture was concentrated. The white solid obtained was treated with methanol (14 mL), followed by hydrogen chloride (2M in diethyl ether, 14 mL). The resulting mixture was heated to reflux for 2 hours, allowed to cool to ambient temperature and then concentrated at reduced pressure. To the residue was added aqueous hydrochloric acid (10 mL, 1 N) followed by diethyl ether (20 mL). The aqueous layers were separated and concentrated at reduced pressure and dried to give the product as a white solid (796 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609849B1 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-8f57ebd270e84c4d953e39518ff6d135 |
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| Source note | uspto-grants-2013_12 |
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