HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918192Generated: October 30, 2026
Isatoic Anhydride → N-(p-fluorobenzyl)isatoic anhydride
https://huagongshe.com/reaction/918192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(p-fluorobenzyl)isatoic anhydride | HCID 12223278 | — |
Reaction Steps
To a solution of 3.2 kgs. isatoic anhydride in 15 kgs. dimethylacetamide is added under nitrogen with stirring sodium hydride obtained from 880 gms. of a 57% dispersion in mineral oil, while maintaining the temperature below 25°C. The resulting mixture is heated to about 60°C. and held at about 55°-60°C. for 1 hour. The reaction mixture is then cooled to 20°-30°C. and to it is added 3.0 kgs. p-fluorobenzyl chloride. The mixture is then reheated to about 60°C. and held there for about 4 hours. It is then cooled again to 20°C. and to it is added 17.4 kgs. of ice and then 24 kgs. water. The mixture is stirred for 15 minutes, the solids collected by filtration, washed with several 2 kg. portions of water and then three times with 0.7 kg. diethylether. The washed solids are dried to obtain N-(p-fluorobenzyl)isatoic anhydride, m.p. 140°-143°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03969506 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-de241e202ab142e38d484ca9443ab576 |
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| Source note | uspto-grants-1976_07 |
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