HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230786Generated: October 29, 2026
Tetrahydrofuran → HCID 68998953, compound
https://huagongshe.com/reaction/230786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,3-Thiazole-2-carbaldehyde | HCID 2734903 | — |
| Reactant | 4-[(Diethoxyphosphoryl)methyl]benzoic acid | HCID 13745801 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68998953 | HCID 68998953 | 1.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566781B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-7d7945097bf14eb2bdbe16916d7bc4c4 |
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| Source note | uspto-grants-2009_07 |
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