HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258823Generated: October 26, 2026
Acetic Anhydride → N-{4-[(4-benzhydryl-1-piperidinyl)methyl]phenyl}acetamide
https://huagongshe.com/reaction/258823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-{[4-(Diphenylmethyl)-1-piperidinyl]methyl}benzenamine | HCID 20225820 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-{4-[(4-benzhydryl-1-piperidinyl)methyl]phenyl}acetamide | HCID 21424837 | — |
Reaction Steps
To a solution of 8 parts of 4-{[4-(diphenylmethyl)-1-piperidinyl]methyl}benzenamine in 50 parts of acetic acid is added 5 parts of acetic anhydride. The resultant mixture is heated to the boiling point under reflux and maintained thereat for 10 minutes, then stripped of solvents by vacuum distillation. The residue is combined with 10 volumes of water. The resultant mixture is made alkaline with concentrated ammonium hydroxide. The mixture thus obtained is extracted with dichloromethane. The dichloromethane extract is dried over anhydrous potassium carbonate and then stripped of solvent by vacuum distillation. The residue, recrystallized from benzene, affords N-acetyl-4-{[4-(diphenylmethyl)-1-piperidinyl]methyl}benzenamine melting at approximately 182°-183°. The product has the formula ##STR5##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04035372 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-d664fea9c1b846caac6ca05eb08f8072 |
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| Source note | uspto-grants-1977_07 |
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