HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043760Generated: October 30, 2026
Triethylamine → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine
https://huagongshe.com/reaction/2043760
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine | HCID 4184869 | 89.5% |
Reaction Steps
To a solution of 1,1-dimethylethyl 4-hydroxy-1-piperidinecarboxylate (4.02 g, 20 mmol) and triethylamine (4.4 mL) in 50 mL of dichloromethane was slowly added methanesulfonylchloride (1.7 mL, 22 mmol) at 0° C. The reaction mixture was stirred for 1 h at 0° C., washed with 1 M aqueous hydrochloric acid, dried over MgSO4 and concentrated in vacuo to give 5 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586611B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-e3dc494e0cb74936b82b9f793167ef4e |
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| Source note | uspto-grants-2013_11 |
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