HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344877Generated: October 30, 2026
Water → 3-chloro-N-(3,4-difluorophenyl)propanamide
https://huagongshe.com/reaction/344877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | 3,4-Difluoroaniline | HCID 77469 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-chloro-N-(3,4-difluorophenyl)propanamide | HCID 3471403 | 95.4% |
Reaction Steps
3-Chloropropionyl chloride (139.16 g) is added with stirring in the course of 1 hour and a half to a solution, heated to a temperature in the region of 55° C., of 3,4-difluoroaniline (125 g) in pyridine (80 cc) and acetone (1.5 liters), and the mixture is maintained at this temperature for 1 hour and a half. After cooling to approximately 20° C., the solution is poured with stirring into a mixture of water (1 liter) and crushed ice (500 g). The temperature is allowed to rise to approximately 20° C. and the product is extracted with dichloromethane (3×500 cc). The combined organic extracts are washed with N hydrochloric acid (500 cc) and water (5×500 cc), dried over magnesium sulphate, filtered and concentrated under reduced pressure (20 kPa) at approximately 50° C. The solid obtained is taken up in n-hexane (500 cc), drained and washed with the same solvent (2×100 cc). 3',4'-Difluoro-3-chloropropionanilide (202.9 g) is obtained in the form of a beige solid, m.p. 76° C., which is used without further purification for the subsequent steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05053509 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-10e65b65d28f4eb1b49ab675f44dc575 |
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| Source note | uspto-grants-1991_10 |
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