HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354025Generated: November 1, 2026
Triethylamine → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine
https://huagongshe.com/reaction/2354025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine | HCID 4184869 | — |
Reaction Steps
To 300 ml of an ethyl acetate solution containing 30.00 g of N-t-butoxycarbonyl-4-hydroxypiperidine and 41.6 ml of triethylamine was added dropwise 17.3 ml of mesyl chloride at −10° C. over 10 minutes. The temperature increased to 5° C. due to heat generation. After stirring with cooling in an ice bath for 10 minutes, 90 ml of water was carefully added dropwise to the reaction mixture. The temperature increased from 0° C. to 6° C. due to heat generation. After stirring for 10 minutes, the mixture was separated and the organic phase washed with water (90 ml×2), saturated saline (90 ml), water (90 ml) and saturated saline (90 ml) in this order. After drying with anhydrous magnesium sulfate, concentration was conducted under reduced pressure and 40.74 g of 1-t-butoxycarbonyl-4-mesyloxypiperidine was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750156B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-583c4432629f4a7dbd167032777513a1 |
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| Source note | uspto-grants-2010_07 |
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