HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815145Generated: October 30, 2026
Methanesulfonyl chloride → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1815145
Participants
| Role | Name | HCID | Charge |
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| 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/1N 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 | US06878714B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-e32a54bbe57b49ca9ebeeda4d7537e8f |
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| Source note | uspto-grants-2005_04 |
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