HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414591Generated: October 29, 2026
Ethyl chloroacetate → HCID 67857985, compound
https://huagongshe.com/reaction/414591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10797035 | HCID 10797035 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67857985 | HCID 67857985 | 46.3% |
Reaction Steps
A solution of N-(1H-pyrrol-1-yl)-4-pyridinamine (5 g) in 25 ml of dimethylformamide was slowly added to a suspension of sodium hydride (60% oil dispersion, 1.4 g, washed with hexane) in 5 ml of dimethylformamide. After the anion formation, the mixture was cooled with an ice-salt bath, and a solution of ethyl chloroacetate (4.2 g) in 5 ml of dimethylformamide was slowly added. After thirty minutes, the mixture was stirred with ice water and extracted with dichloromethane. The organic extract was washed with water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated to 8 g of oil. This oil was purified by HPLC (silica, ethyl acetate) to give 4.1 g of solid, mp 92°-95°. This material was converted to the hydrochloride salt and recrystallized twice from isopropanol and once from ethanol to give 2.6 g of crystals, d 240°-241°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04792562 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-bcbc5904dc024b64aa5872afe8e43d6c |
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| Source note | uspto-grants-1988_12 |
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