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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691832Generated: November 1, 2026

trans-1-Methoxy-3-trimethylsilyloxy-1,3-butadiene → 1-(2-trimethylsilyl-ethanesulfonyl)-2,3-dihydro-1H-[2,3']bipyridinyl-4-one

https://huagongshe.com/reaction/1691832

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 5366448—
Reactant2-Trimethylsilyl-ethanesulfonic acid pyridin-3-ylmethyleneamideHCID 66907499—
SolventTolueneHCID 1140—
Product1-(2-trimethylsilyl-ethanesulfonyl)-2,3-dihydro-1H-[2,3']bipyridinyl-4-oneHCID 5937776140%

Reaction Steps

To a solution of 2-trimethylsilyl-ethanesulfonic acid pyridin-3-ylmethyleneamide (665 mg) in toluene (4.5 mL) was added Danishefsky's diene (0.46 mL, 2.4 mmol) under Ar atmosphere. The mixture was heated at reflux for 90 minutes. The toluene was removed in vacuo and the residue was dissolved in dichloromethane (ca. 10 mL) and treated with 2N HCl (ca. 10 mL) for 5 minutes. 10% Aqueous sodium bicarbonate was added carefully to adjust to pH 8. The phases were separated and the aqueous phase was extracted with dichloromethane. The combined organic extracts were dried (Na2SO4), filtered and evaporated to dryness under reduced pressure. Purification of the residue by flash chromatography (gradient hexane/ethyl acetate) gave 1-(2-trimethylsilyl-ethanesulfonyl)-2,3-dihydro-1H-[2,3′]bipyridinyl-4-one (322 mg, 40% overall).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153809B2
Source datasetuspto-grants-2012_04
ORD IDord-38e7220ae01b4dd0a0d01cb1ec3efad7
Source noteuspto-grants-2012_04