HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231559Generated: October 26, 2026
Acetyl chloride → 3-Chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dione
https://huagongshe.com/reaction/231559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | 3-(Chloromethyl)oxolane-2,5-dione | HCID 13592830 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dione | HCID 20033479 | 93% |
Reaction Steps
In a variant of (b), into a toluene solution of 33.3 g (0.3 moles) 4-fluoroaniline, a toluene solution of 44.6 g (0.3 moles) 2-chloromethylsuccinic acid anhydride were added dropwise at room temperature while stirring. The temperature of the mixture rose to 40° C. during the operation. To the suspension of the semi-anilide obtained, 0.35 moles of acetylchloride was added dropwise at 60° C. while stirring, the addition being carried out so slowly that the ensuing gas development could be easily controlled. After 3 hours the reaction mixture was heated to 100° C. and held at that temperature until the gas development was terminated. The semi-anilide thereby dissolved. When the reaction mixture was cooled down, the desired product crystallized. The actual yield was 93% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04847285 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-384911e3274b45318b1e9fd76d82376d |
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| Source note | uspto-grants-1989_07 |
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