HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929471Generated: November 1, 2026
Chloroacetyl chloride → HCID 58155316, compound
https://huagongshe.com/reaction/1929471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58155345 | HCID 58155345 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58155316 | HCID 58155316 | — |
Reaction Steps
(RS)-2-Amino-2-(5-bromo-2-fluoro-phenyl)-2-cyclopropyl-ethanol (2.27 g, 8 mmol) was dissolved in a mixture of dichloromethane (85 ml) and a saturated aqueous solution of sodium hydrogen-carbonate (85 ml). The biphasic mixture was then treated with a solution of chloroacetylchloride (0.69 ml, 8.7 mmol) in dichloromethane. The reaction mixture was stirred at room temperature and the progress of the transformation checked by chromatography. After completion, the reaction mixture was diluted with dichloromethane, the organic layer separated and washed with water, then dried over sodium sulfate and evaporated. The (RS)-N-[1-(5-bromo-2-fluoro-phenyl)-1-cyclopropyl-2-hydroxy-ethyl]-2-chloro-acetamide was obtained as a yellow oil (2.73 g, 94.0% of theory). Mass (calculated) C13H14BrClFNO2 [350.614]; (found) [M+H]+=350, [M+2-H]+=352, [M+4-H]+=354.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188079B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-da8b01d30a9946bc8e7a772f7c162677 |
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| Source note | uspto-grants-2012_05 |
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