HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854110Generated: October 30, 2026
Dichloromethane → Methyl 4-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/854110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 45123042 | 90% |
Reaction Steps
4-Hydroxymethylpiperidine (47.6 g, 1.0 eq) and water (300 mL) were charged to a flask. The resulting mixture was cooled to 0-10° C. Potassium carbonate (85.7 g, 1.5 eq) dissolved in water (150 mL) and methyl chloroformate (38.4 mL, 1.1 eq) were added while maintaining the temperature at below 10° C. When the addition was complete, the reaction mixture was warmed up to 20-30° C. for 1 hour. After the reaction was complete, dichloromethane (500 mL) was added to the reaction mixture. The organic layer was collected and washed with 1 M phosphoric acid solution (200 mL), saturated sodium bicarbonate solution (200 mL) and saturated sodium chloride solution (200 mL). The organic layer was dried over sodium sulfate (50 g, 1 w/w eq) and then distilled under vacuum to produce the title intermediate. (67.0 g, 90% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256294B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-e338e2d31afd40ff9573b39743243392 |
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| Source note | uspto-grants-2007_08 |
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