HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620257Generated: October 29, 2026
Chloroacetonitrile → HCID 14116886, compound
https://huagongshe.com/reaction/620257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | 4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-hydroxybenzamide hydrochloride | HCID 14116877 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14116886 | HCID 14116886 | 57.3% |
Reaction Steps
To a stirred suspension of sodium hydride (420 mg of 60%, 10.5 mmoles, washed with n-pentane) in 10 ml DMF was added 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide hydrochloride (1.612 g, 5 mmoles) and the mixture stirred for 20 minutes, followed by cooling (ice bath) and addition of chloroacetonitrile (418 mg, 5.5 mmoles) and sodium bromide (100 mg). The mixture was stirred in the cold for 1 hour and at ambient temperature for 16 hours, followed by pouring into a mixture of water and ice, and filtration of the resulting solid. The product was dissolved in methylene chloride and filtered over alumina, followed by concentration in vacuo to give crude product. This was recrystallized from methanol to give 930 mg (57%) of the title compound as white crystalline solid mp 188°-189°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ 8.1 (s, 1H); 7.78 (bs, 1 H); 6.44 (s, 1H); 4.84 (s, 2H); 4.60 (s, 2H); 3.43 (m, 2H); 2.59 (m, 6H); 1.02 (t, 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-ba8d827d987e4f868c5e73eaab5e59cf |
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| Source note | uspto-grants-1989_04 |
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