HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231206Generated: October 31, 2026
Chloroacetyl chloride → HCID 14257921, compound
https://huagongshe.com/reaction/2231206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 68770-54-7 | HCID 20396933 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 14257921 | HCID 14257921 | 74.5% |
Reaction Steps
Triethylamine (254.9 g, 2.5 mol) was added with stirring to a solution of 1-phenyl-2-(3-methoxyphenyl)ethylamine hydrochloride (166.0 g, 0.63 mol) in chloroform (4 L) under nitrogen at 0° C. Then chloroacetyl chloride (142.2 g, 1.26 mol) was added dropwise over a period of 2 hrs. The resulting mixture was stirred at ambient temperature (about 25° C.) for 16 hrs, washed with 10% HCl (3×1 L) and water (1 L), and then the organic phase was dried over MgSO4. Evaporation of the solvent gave a dark oily residue which was dissolved in cyclohexane (2 L). Upon standing, the resulting solution gave solid crystals which were collected by filtration and dried to give 142.5 g of N-chloroacetyl-1-phenyl-2-(3-methoxyphenyl)ethylamine. A sample recrystallized twice from cyclohexane had a mp. 104°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04782058 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-11cf446c102d4d4bbf6446e0f995196d |
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| Source note | uspto-grants-1988_11 |
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