HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076967Generated: November 1, 2026
N-Hydroxyphthalimide → HCID 21535544, compound
https://huagongshe.com/reaction/1076967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Difenoxin | HCID 34328 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21535544 | HCID 21535544 | — |
Reaction Steps
2.12 Grams of 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylic acid are dissolved in 65 ml. of redistilled N,N-dimethylformamide by warming to about 60°C. To the warm solution is added, with stirring, .82 gram of N-hydroxyphthalimide, followed by 1.16 grams of dicyclohexylcarbodiimide. The resultant mixture is stirred at room temperature under calcium chloride, then cooled and filtered. The filtrate is diluted with water and extracted with ethyl acetate. The ethyl acetate layer is washed with water, dried over potassium carbonate and partially concentrated until a precipitate forms. Filtration and repeated crystallizations of the precipitate from a mixture of chloroform and hexane affords N-[1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carbonyloxy]phthalimide, melting at about 156.5°-157.5°C. The product has the formula ##SPC4##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03959275 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-a81f3c8de6b249958b1210198ef785f2 |
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| Source note | uspto-grants-1976_05 |
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