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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Acetyl-4-hydroxy-4-tributylstannyl-piperidine | HCID 15636899 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(Tributylstannyl)-3,6-dihydropyridin-1(2H)-yl]ethan-1-one | HCID 15636896 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04945160 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-e7279b2515a4451cac7ec3db49515000 |
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| Source note | uspto-grants-1990_07 |
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