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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166496Generated: October 31, 2026

Triethylamine → 1-[4-(Tributylstannyl)-3,6-dihydropyridin-1(2H)-yl]ethan-1-one

https://huagongshe.com/reaction/2166496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Acetyl-4-hydroxy-4-tributylstannyl-piperidineHCID 15636899—
SolventDichloromethaneHCID 6344—
Product1-[4-(Tributylstannyl)-3,6-dihydropyridin-1(2H)-yl]ethan-1-oneHCID 15636896—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Acetyl-4-hydroxy-4-tributylstannyl-piperidine, 20 (16.4 g, 38 mmol) and triethylamine (15.0 ml, 108 mmol) were dissolved in methylene chloride (250 ml) and the solution cooled to 0° C. Methanesulfonylchloride (6.0 ml, 50 mmol) in methylene chloride (50 ml) was added dropwise to the cooled solution and the mixture was allowed to warm to room temperature and stir for 60 hours. The reaction solution was washed with NaCl solution, dried (MgSO4), filtered, and evaporated to give a red oil which was purified by flash column chromatography on silica gel, eluting with 3% ethanol in CH2Cl2. After combining the appropriate fractions and evaporating the solvent, the title compound, 21, was obtained (7.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945160
Source datasetuspto-grants-1990_07
ORD IDord-e7279b2515a4451cac7ec3db49515000
Source noteuspto-grants-1990_07