HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464661Generated: October 30, 2026
Ethyl chloroformate → Ethyl 4-(4-fluorobenzoyl)-4-phenylpiperidine-1-carboxylate
https://huagongshe.com/reaction/464661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | (4-Fluorophenyl)[4-phenyl-1-(phenylmethyl)-4-piperidinyl]methanone | HCID 15586470 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4-(4-fluorobenzoyl)-4-phenylpiperidine-1-carboxylate | HCID 13477817 | — |
Reaction Steps
To a stirred mixture of 79 parts of (4-fluorophenyl)[4-phenyl-1-(phenylmethyl)-4-piperidinyl]methanone and 630 parts of methylbenzene were added dropwise 32 parts of ethyl carbonochloridate at room temperature. Upon completion, stirring was continued for 5 hours at reflux temperature. The reaction mixture was evaporated and the (chloromethyl)benzene was distilled in vacuo (pump). The oily residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2,2'-oxybispropane and a small amount of petroleumether, yielding 35.5 parts of ethyl 4-(4-fluorobenzoyl)-4-phenyl-1-piperidinecarboxylate; mp. 91.7° C. (intermediate 15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548938 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-0dd67b3509f34a90bb0b0173c003226e |
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| Source note | uspto-grants-1985_10 |
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