HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213012Generated: October 26, 2026
Water → 1,1-Dimethylethyl 4-Hydroxymethyl-4-methanesulfonyloxymethyl-1-piperidinecarboxylate
https://huagongshe.com/reaction/2213012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Tert-butyl 4,4-bis(hydroxymethyl)piperidine-1-carboxylate | HCID 21955203 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-Dimethylethyl 4-Hydroxymethyl-4-methanesulfonyloxymethyl-1-piperidinecarboxylate | HCID 17979980 | 54.1% |
Reaction Steps
Methanesulfonyl chloride (44 μL, 0.56 mmol) in dichloromethane (10 mL) was added slowly to a stirred, cooled (0° C.) solution of 1,1-dimethylethyl 4,4-bis(hydroxymethyl)-1-piperidinecarboxylate (Description 67, 140 mg, 0.56 mmol) and triethylamine (95 μL, 0.68 mmol) in dichloromethane (50 mL). The mixture was allowed to warm to room temperature and stirred for 16 hours. Water (10 mL) was added and the layers were separated. The aqueous layer was extracted with dichloromethane (2×40 mL), the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (80:20 increasing to 0:100), to give the title compound (98 mg, 54%). m/z (ES+) 324 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105507B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-10610de2250b47a9a710fed64b01bc17 |
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| Source note | uspto-grants-2006_09 |
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