HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681808Generated: November 2, 2026
Potassium Cyanide → 2-Amino-2-(3-bromophenyl)acetonitrile hydrochloride
https://huagongshe.com/reaction/1681808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-2-(3-bromophenyl)acetonitrile hydrochloride | HCID 17979643 | — |
Reaction Steps
A solution of 3-bromobenzaldehyde (18.5 g, 0.1 mol) is dissolved in methanol (15 ml) and stirred at room temperature as a solution of ammonium chloride (5.35 g, 0.1 mol) in water (12.5 ml) is added in one portion. After thirty minutes a solution of potassium cyanide (6.5 g, 0.1 mol) in water (12.5 ml) is added in one portion and the reaction stirred overnight. The mixture is then refluxed one hour, allowed to cool, and the separated oil extracted into diethyl ether and treated with an ethereal solution of hydrogen chloride to give a brown solid. This is recrystallized by dissolving in methanol (100 ml), diluting with diethyl ether (450 ml), and refrigerating the solution overnight. The solid obtained is filtered, washed with ether, and dried (3.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175153 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-056bc687e06c4507b0ae3be950f09506 |
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| Source note | uspto-grants-1992_12 |
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