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
Participants
| Role | Name | HCID | Charge |
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| Reactant | trans-1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 5366448 | — |
| Reactant | 2-Trimethylsilyl-ethanesulfonic acid pyridin-3-ylmethyleneamide | HCID 66907499 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-trimethylsilyl-ethanesulfonyl)-2,3-dihydro-1H-[2,3']bipyridinyl-4-one | HCID 59377761 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153809B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-38e7220ae01b4dd0a0d01cb1ec3efad7 |
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| Source note | uspto-grants-2012_04 |
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