HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846742Generated: October 31, 2026
Dichloromethane → Ethyl 3-(benzyloxy)-4-oxopiperidine-1-carboxylate
https://huagongshe.com/reaction/846742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 15096753 | HCID 15096753 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 3-(benzyloxy)-4-oxopiperidine-1-carboxylate | HCID 3019711 | 86.5% |
Reaction Steps
To a stirred mixture of 10 parts of 3-(phenylmethoxy)-1-(phenylmethyl)-4-piperidinone and 65 parts of dichloromethane were added dropwise 5 parts of ethyl carbonochloridate at room temperature. After stirring for 6.30 hours at reflux, there were added 5 parts of N,N-diethylethanamine. Upon completion, stirring at reflux was continued for 24 hours. The reaction mixture was washed successively with water, a diluted hydrochloric acid solution and again with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 8.1 parts (86.5%) of ethyl 4-oxo-3-(phenylmethoxy)-1-piperidinecarboxylate as an oily residue (intermediate 47).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137896 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-f1663116453c4c75aed1d5bdd25dcaf3 |
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| Source note | uspto-grants-1992_08 |
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