HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196331Generated: October 29, 2026
Chloroacetyl chloride → N-(2-(5-bromo-2-fluorophenyl)-3,3-difluoro-4-hydroxybutan-2-yl)-2-chloroacetamide
https://huagongshe.com/reaction/2196331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 66666062 | HCID 66666062 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-(5-bromo-2-fluorophenyl)-3,3-difluoro-4-hydroxybutan-2-yl)-2-chloroacetamide | HCID 66665738 | — |
Reaction Steps
To an ice cooled solution of 3-amino-3-(5-bromo-2-fluorophenyl)-2,2-difluorobutan-1-ol (3.1 g, 10.4 mmol), in DCM (60 ml) was added aqueous Na2CO3 (2.74 g, 25.8 mmol in 7.0 mL H2O) and stirred for 10 min. Chloroacetyl chloride (0.986 ml, 11.4 mmol) was then added to the resultant reaction mixture and stirring continued for 30 min at 0° C. Upon formation of the new product by TLC analysis, K2CO3 (1.5 g, 10.4 mmol) in MeOH (17 mL) was added to the reaction mixture and stirred at rt for 30 min. The reaction mixture was diluted with DCM, separated the organic layer and washed successively with water and brine solution, dried over anhydrous Na2SO4 and concentrated under reduced pressure to furnish title compound as a colorless gum. Yield=3.3 g (78.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338413B1 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-9e4862a82fba45428c078c1fca55331d |
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| Source note | uspto-grants-2012_12 |
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