HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035306Generated: October 31, 2026
Triethylamine → Methanesulfonic acid 1-methoxy-piperidin-4-yl ester
https://huagongshe.com/reaction/2035306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Methoxypiperidin-4-ol | HCID 3022606 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methanesulfonic acid 1-methoxy-piperidin-4-yl ester | HCID 86663299 | 126.3% |
Reaction Steps
21 g 1-Methoxy-piperidin-4-ol (from Step 1) and 19.4 g triethylamine were dissolved in 200 ml ethyl acetate, and cooled to 0° C. 15.0 g Methanesulfonyl chloride was added slowly. The resulting white suspension was stirred at 0° C. for 1 hour, then at room temperature for an additional 1 hour. Then the mixture was filtered and the solvent evaporated, yielding 34.6 g of methanesulfonic acid 1-methoxy-piperidin-4-yl ester. This material was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574607B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-a4235c195d2e4a28a2782dc713e599bd |
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| Source note | uspto-grants-2013_11 |
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