HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973827Generated: November 2, 2026
Butyric anhydride → N-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioate
https://huagongshe.com/reaction/1973827
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyric anhydride | HCID 7798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Piperidinamine, 4-(methoxymethyl)-N-phenyl-1-(2-phenylethyl)- | HCID 12298210 | — |
| Product | N-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioate | HCID 12298012 | — |
Reaction Steps
A mixture of 3 parts of 4-(methoxymethyl)-N-phenyl-1-(2-phenylethyl)-4-piperidinamine and 5 parts of butanoic acid, anhydride is stirred and refluxed for 8 hours. The reaction mixture is poured onto water and the whole is alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is stirred in 1,1'-oxybisethane with activated charcoal. The latter is filtered off and the filtrate is evaporated. The residue is converted into the ethanedioate salt 2-propanol. The salt is filtered off and crystallized from 2-propanone, yielding 1.7 parts of N-[4-(methoxymethyl)-1-(2-phenylethyl)-4-piperidinyl]-N-phenylbutanamide ethanedioate; mp. 174.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998834 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-e7b2f4470f2347e5b5c96e42c0487cd5 |
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| Source note | uspto-grants-1976_12 |
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