HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324307Generated: October 25, 2026
Chloroacetyl chloride → HCID 18623236, compound
https://huagongshe.com/reaction/324307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Amino-2-(3,4-difluorophenyl)ethanol | HCID 22048878 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18623236 | HCID 18623236 | — |
Reaction Steps
To a solution of 2-amino-2-(3,4-difluorophenyl)-ethanol 2.6 g, 15.0 mmol) in CH2Cl2 (15 mL) and 20% (by wt.) NaOH (15 mL) was added a solution of chloroacetyl chloride (1.32 mL, 16.5 mmol) in 15 mL of CH2Cl2 at −10° C. dropwise under argon atmosphere. After the addition was complete, the reaction mixture was stirred for 15 min and then it was transferred to a separatory funnel. The organic layer was separated and the aqueous layer was extracted with CH2Cl2 (2×20 mL). The combined organic extracts were washed with a solution containing 10 mL of brine and 5 drops of concentrated HCl. The organic layer was dried over MgSO4, filtered and the solvent was removed in vacuo to give a white solid. It was further purified with flash column chromatography on silica gel with 1:1 hexane/EtOAc followed by EtOAc as the eluting system. 2-Chloro-N-[1-(3,4-difluorophenyl)-2-hydroxy-ethyl]-acetamide was obtained as a white solid (2.6 g, 69.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218390B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-2e45fa0dc5ba46549bc72cceacaa6eca |
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| Source note | uspto-grants-2001_04 |
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