HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550815Generated: October 30, 2026
1-Benzyl-4-piperidone → 1-PIPERIDINECARBONYL CHLORIDE, 4-OXO-
https://huagongshe.com/reaction/550815
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-PIPERIDINECARBONYL CHLORIDE, 4-OXO- | HCID 11829745 | 251.4% |
Reaction Steps
A solution of triphosgene (2.84 g, 9.6 mmol) in methylene chloride (100 mL) at 0° C. was treated with a solution of 1-benzyl-piperidin-4-one (6.0 g, 31.7 mmol) in methylene chloride (100 mL). The reaction mixture was allowed to warm to 25° C. and was stirred at 25° C. overnight. At this time, the mixture was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, gradient elution 60/40 ethyl acetate/hexanes) afforded 4-oxo-piperidine-1-carbonyl chloride (3.9 g, 76%) as a brown oil. The NMR spectrum obtained on the sample is compatible with its structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947692B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-c97fa9e3bcfa41a69b3efcc92cfb9657 |
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| Source note | uspto-grants-2011_05 |
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