HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417469Generated: October 28, 2026
Benzoyl chloride → Benzyl 9-benzoyl-1,2,3,4-tetrahydrocarbazole-3-carboxylate
https://huagongshe.com/reaction/1417469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 9-benzoyl-1,2,3,4-tetrahydrocarbazole-3-carboxylate | HCID 54294365 | — |
Reaction Steps
A solution of 291 mg of benzyl 1,2,3,4-tetrahydrocarbazole-3-carboxylate, as obtained in Example 50, in 2 ml of N,N-dimethylformamide was added, with ice-cooling, to a suspension of 87 mg of sodium hydride (55% w/w dispersion in mineral oil) in 4 ml of N,N-dimethylformamide. 0.12 ml of benzoyl chloride was added to the reaction mixture which was then stirred for 1 hour. After this time, a saturated aqueous solution of ammonium chloride was added to the reaction mixture. The aqueous layer was extracted with ethyl acetate, and the organic extract was washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The resulting residue was subjected to column chromatography using 10 g of silica gel with a 5:1 v/v mixture of hexane and ethyl acetate as the eluent, to yield 384 mg of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877199 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-1fd870dffa0b4777ada4ec21ff2ce7f4 |
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| Source note | uspto-grants-1999_03 |
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