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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260284Generated: November 1, 2026

Tetrahydrofuran → HCID 67345946, compound

https://huagongshe.com/reaction/1260284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-AcetylpyridineHCID 9589—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylphosphonoacetateHCID 53413272—
ProductHCID 67345946HCID 67345946—

Reaction Steps

Sodium hydride (192 mg of a 60% wt. suspension, 4.80 mmol) was added in several portions to a stirred solution of trimethylphosphonoacetate (712 μL, 4.40 mmol) in THF (20.0 mL). After 5 min, 1-pyridin-3-ylethanone (440 μL, 4.00 mmol) was added dropwise, and the resulting mixture was heated to reflux. After 20 h, the reaction mixture was cooled to rt, poured into satd. aq. NH4Cl and extracted with EtOAc. The combined organics were washed with brine, dried (sodium sulfate) and concentrated in vacuo. Purification of the crude residue by flash chromatography on silica gel (gradient elution; 0%-60% EtOAc/hexanes as eluent) afforded the title compound i-7a as a separable mixture of two isomers. m/z (ES) 178 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470819B2
Source datasetuspto-grants-2013_06
ORD IDord-11c6988c0a044d49a0142976e6bbe0cc
Source noteuspto-grants-2013_06