HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211617Generated: November 1, 2026
Methanesulfonyl chloride → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/2211617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 2764081 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate | HCID 2765838 | — |
Reaction Steps
Dissolved 1-Boc-4-hydroxymethyl-piperidine in anhydrous CH2Cl2 (50 mL) and TEA (4.5 mL) and cooled to 0° C. Mesyl chloride (840 μl) was added and the mixture was stirred for 15 min then at RT for 45 min. The mixture was washed with brine/1 N HCl and then brine, dried over Na2SO4, concentrated in vacuo and dried under high vacuum to provide 1-Boc-4-methylsulfonyloxymethyl-piperidine as a yellow orange thick oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101868B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-274bcc7a87614b42b84d436adfb9656d |
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| Source note | uspto-grants-2006_09 |
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