HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639523Generated: November 2, 2026
Sodium Cyanide → 2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamine hydrochloride
https://huagongshe.com/reaction/639523
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzyl bromide | HCID 2778114 | — |
| Reactant | 2-(4-Chloro-3-(trifluoromethyl)phenyl)acetonitrile | HCID 5004685 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamine hydrochloride | HCID 68560752 | — |
Reaction Steps
A mixture of 4-bromomethyl-1-chloro-2-trifluoromethyl-benzene (3.94 g, 14.4 mmol) and sodium cyanide (1.06 g, 21.6 mmol) in dimethyl sulfoxide (12 mL) was heated at 50° C. for one hour. The reaction mixture was then poured on ice water and extracted four times with dichloromethane. The combined organic phases were washed with water, dried over magnesium sulfate, filtered and concentrated, leading to (4-chloro-3-trifluoromethyl-phenyl)-acetonitrile (3.19 g, 14.4 mmol) as a dark red oil. This crude material was transformed into the title compound in accordance with the general method of example H2. White solid, MS (ISP) 224.1 (M−Cl)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691876B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-54f84f45b84d4484bbd2c61b7056c7d3 |
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| Source note | uspto-grants-2010_04 |
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