HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454364Generated: October 30, 2026
Hydrochloric Acid → 3-Amino-1-(3-bromophenyl)propan-1-ol
https://huagongshe.com/reaction/454364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(3-Bromophenyl)-3-hydroxypropanenitrile | HCID 57608363 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-1-(3-bromophenyl)propan-1-ol | HCID 57608334 | — |
Reaction Steps
To a solution of 3-(3-bromophenyl)-3-hydroxypropanenitrile (23) (117.5 g, 519.8 mmol) in anhydrous THF (300 mL) under argon borane-methylsulfide (68 mL, 675.7 mmol) was slowly added over 30 min via a dropping funnel. The reaction mixture was boiled under reflux for 2.5 hr and cooled to room temperature. HCl solution (1.25M in EtOH, 350 mL) was slowly added for 30 min and the mixture was concentrated under reduced pressure. Water (400 mL) was added and the pH of the mixture was then adjusted to 12 with aqueous NaOH (50% wt). The product was extracted with CH2Cl2 (500 mL), the extract was dried over anhydrous Na2SO4 and concentrated under reduced pressure to give hydroxyamine 24 as a colorless oil. Yield (104 g, 87%). 1H NMR (400 MHz, DMSO-d6) δ 7.49 (m, 1H), 7.37 (dt, J=7.2, 1.6 Hz, 1H), 7.23-7.31 (m, 2H), 4.66 (t, J=6.8 Hz, 1H), 2.61 (m, 2H), 1.61 (q, J=6.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492589B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-82692e7993414e80ae4796d8e8ae0d94 |
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| Source note | uspto-grants-2013_07 |
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