HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901342Generated: October 29, 2026
Hydrochloric Acid → 1-Phenylpropan-1-amine
https://huagongshe.com/reaction/901342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 11367260 | HCID 11367260 | — |
| Reactant | 3-[3-(Trifluoromethyl)phenyl]propan-1-amine | HCID 19797640 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Titanium isopropoxide | HCID 11026 | — |
| Product | 1-Phenylpropan-1-amine | HCID 18054 | 240.4% |
Reaction Steps
The mixture of 1-(7,8-dihydro-naphthalen-1-yl)-ethanone (10) (172 mg, 1.0 mmol) and 3-(3-trifluoromethyl-phenyl)-propylamine (13) (204 mg, 1.0 mmol) in titanium (IV) isopropoxide (1 mL) was stirred at room temperature overnight. Methanol(5 mL) was added followed by addition of sodium borohydride (55 mg, 2.0 mmol). The reaction mixture was stirred at room temperature for 1 hour and evaporated to dryness. The crude product was purified by chromatography on silica gel, loaded with dichloromethane and eluted with 2% methanol in dichloromethane containing 0.5% ammonium hydroxide. The pure fractions were combined and evaporated to give a colorless oil. The product was converted to a hydrochloride salt by addition of 1 N HCl in ethyl ether. Evaporation gave compound (1) as an off-white solid (325 mg, 82.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361789B1 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-5b464b77cffb46488b0b0d07513a59eb |
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| Source note | uspto-grants-2008_04 |
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