HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688112Generated: November 1, 2026
Chloroacetyl chloride → 2-Chloro-N-methyl-N-(2-phenylethyl)acetamide
https://huagongshe.com/reaction/1688112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylbenzeneethanamine | HCID 11503 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-N-methyl-N-(2-phenylethyl)acetamide | HCID 12557952 | 95% |
Reaction Steps
At −75° C., chloroacetyl chloride (11.3 g, 8.1 mL, 0.1 mol) was added slowly to a suspension of methyl-phenethyl-amine (13.5 g, 0.1 mol), triethylamine (15 mL) in dichloromethane (50 mL). The suspension was warmed to 25° C. over the course of 3 hours and the salt was removed by filtration. The organic phase was washed with HCl solution (1 N, 200 mL), dried with sodium sulfate. The solvent was evaporated in vacuo to give 2-chloro-N-methyl-N-phenethyl-acetamide (20 g, 95%): 1H NMR (300 MHz, CDCl3) δ 7.2 (m, 5H), 4.03 (s, 3H), 3.6 (m, 2H), 2.99 (s, 2H), 2.8 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148391B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-b2c84e1e83e0433fa4d32e4390ae6774 |
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| Source note | uspto-grants-2012_04 |
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