HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463346Generated: October 30, 2026
Chloroacetyl chloride → HCID 20283268, compound
https://huagongshe.com/reaction/463346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2-Diphenylethylamine | HCID 77575 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20283268 | HCID 20283268 | 87.9% |
Reaction Steps
To a stirred solution of 2,2-diphenylethylamine (100.0 g, 0.5 m) and triethylamine (123.0 g, 1.2 m) in chloroform (2 liters) maintained under nitrogen at ambient temperature was added dropwise chloroacetylchloride (124.2 g, 1.1 m) and the mixture stirred for 2 hours. Thin layer chromatography (TLC) analysis showed the reaction to be complete. The mixture was transferred to a separatory funnel and washed with 10% HCl (3×1 liter) and water (1 liter) and the organic phase dried over MgSO4. The solvent was evaporated to a dark oil which was treated with cyclohexane (1 liter) and, upon standing, a solid crystallized which was collected by filtration, washed with cyclohexane and air dried to give 122.0 g of N-chloroacetyl-1,1-diphenylethylamine as a tan solid, m.p. 73°-74°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518779 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-bf4fb4d265f14583b0884c0abfc1569d |
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| Source note | uspto-grants-1985_05 |
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