HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030913Generated: October 29, 2026
Ethanolamine → N-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamide
https://huagongshe.com/reaction/1030913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 1-Benzyl-4-(4-methoxycarbonylphenoxymethyl)piperidin-4-ol | HCID 22291265 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamide | HCID 14989215 | 69.3% |
Reaction Steps
A mixture of 10.7 parts of methyl 4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzoate and 8 parts of 2-aminoethanol was stirred for 4 hours in an oil bath at 145° C. After cooling, the reaction mixture was poured into water. The oil was decanted, washed twice with water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from a mixture of 2,2'-oxybispropane and 2-propanol. The product was filtered off and dried, yielding 8 parts (69.3%) of N-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamide; mp. 161.1° C. (int. 80).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05106973 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-5bb146c736ca4d9eb52ff229ac8364f4 |
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| Source note | uspto-grants-1992_04 |
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