HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620250Generated: October 29, 2026
2-Chloroacetophenone → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(2-oxo-2-phenyl-ethoxy)-benzamide
https://huagongshe.com/reaction/620250
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-hydroxybenzamide hydrochloride | HCID 14116877 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(2-oxo-2-phenyl-ethoxy)-benzamide | HCID 14116890 | 50.1% |
Reaction Steps
To a stirred suspension of sodium hydride (320 mg of 60%, 8 mmoles, washed with n-pentane) in DMF (15 ml) was added 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide hydrochloride (1.289 g, 4 mmoles) and the mixture stirred for 20 minutes followed by addition of chloroacetophenone (619 mg, 4 mmoles). The mixture was stirred 4 hours, poured into ice-cold water (50 ml) whereupon a solid separated out. This was isolated by filtration, dried and recrystallized from methanol to give 810 mg (50%) of the title compound as white solid mp 153°-4°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ 8.64 (bs, 1H); 8.2 (s, 1H); 8 (m, 2H); 7.6 (m, 3H); 6.22 (s, 1H); 5.36 (s, 2H); 4.4 (s, 2H); 3.52 (m, 2H); 2.64 (m, 6H); 1.01 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820715 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-3d0738dd5ebc4d6fb4f22925df2ae2df |
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| Source note | uspto-grants-1989_04 |
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