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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Methoxypiperidin-4-olHCID 3022606—
SolventEthyl AcetateHCID 8857—
ProductMethanesulfonic acid 1-methoxy-piperidin-4-yl esterHCID 86663299126.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08574607B2
Source datasetuspto-grants-2013_11
ORD IDord-a4235c195d2e4a28a2782dc713e599bd
Source noteuspto-grants-2013_11