HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442535Generated: October 30, 2026
Benzoyl chloride → 7-Benzoyl-5-chloroindolin-2-one
https://huagongshe.com/reaction/442535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 5-Chlorooxindole | HCID 152801 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Benzoyl-5-chloroindolin-2-one | HCID 12901223 | — |
Reaction Steps
A mixture of 162.5 g. (1.08 mole) of benzoyl chloride and 260 g. of aluminum chloride (1.80 mole) heated to 200° C. with stirring was treated with 65 g. (.360 mole) of recrystallized 5-chloroindolin-2-one. This mixture was stirred 15 min. and poured over ice. The resulting precipitate was triturated with boiling water and then chloroform. The chloroform solution was washed with 5% sodium bicarbonate, water, dried over sodium sulfate, and stripped to yield approximately 55 g. of a glossy solid. This material was then triturated with hot methanol and the methanol evaporated under vacuum to yield approximately 20 g. of a solid yellow material. Extraction of a benzene solution of this material removed any starting 5-chloroindoline-2-one present and after washing with water and drying the benzene yielded on evaporation 3 g. of a blue-gray material. Trituration of this material with room temperature methanol gave a residue which on recrystallization from methanol yielded 2.5 g. of a tan solid identified as product, m.p. 186°-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04045576 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-eb493980e69c4a5b8790df33688f54f0 |
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| Source note | uspto-grants-1977_08 |
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