HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120006Generated: October 26, 2026
Borane → 3-Amino-1-(thiophen-2-yl)propan-1-ol
https://huagongshe.com/reaction/2120006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | 3-Hydroxy-3-(thiophen-2-yl)propanenitrile | HCID 11252121 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-1-(thiophen-2-yl)propan-1-ol | HCID 12084156 | 81% |
Reaction Steps
To 10 ml of a THF solution of 1.53 g (10 mmol) of the optically active 3-(2-thienyl)-3-hydroxypropanenitrile obtained in Example 6, slowly added was 1.23 ml (13 mmol) of borane.dimethylsulfide complex. After removing the dimethylsulfide by reducing the pressure, the reaction mixture was refluxed for 2.5 hours. The reaction was stopped by addition of a methanol/hydrochloric acid solution, and the methanol was distilled off under vacuum. After neutralizing with a SN aqueous solution of sodium hydroxide, the solvent was distilled off, a further aqueous solution of sodium hydroxide was added to make the reaction solution basic, and this was then extracted with methylene chloride. This methylene chloride solution was dried with anhydrous sodium sulfate, and the solvent was then distilled off under vacuum to give 1.28 g (yield 81%, 1H-NMR) of optically active 1-(2-thienyl)-3-aminopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06686505B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-ddb96b3b28e841a5a33b0dcdfb8f1fc4 |
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| Source note | uspto-grants-2004_02 |
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