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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230786Generated: October 29, 2026

Tetrahydrofuran → HCID 68998953, compound

https://huagongshe.com/reaction/230786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,3-Thiazole-2-carbaldehydeHCID 2734903—
Reactant4-[(Diethoxyphosphoryl)methyl]benzoic acidHCID 13745801—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 68998953HCID 689989531.9%

Reaction Steps

A mixture of 4-(diethoxyphosphorylmethyl)benzenecarboxylic acid (440 mg) produced according to JP-A 11-60537, potassium tert-butoxide (340 mg) and THF (5.5 mL) was stirred at room temperature for about 1.5 hours, and then a THF solution (1.0 mL) of 2-formylthiazole (200 mg) was dropwise added thereto. After heated overnight under reflux, water was added to the reaction solution, and extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated off under reduced pressure. The resulting residue was purified through silica gel column chromatography (ethyl acetate/methanol=9/1), and the resulting purified product was further purified through reversed-phase HPLC to obtain the entitled compound (7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566781B2
Source datasetuspto-grants-2009_07
ORD IDord-7d7945097bf14eb2bdbe16916d7bc4c4
Source noteuspto-grants-2009_07