HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992994Generated: November 1, 2026
Triethyl phosphonoacetate → HCID 67526446, compound
https://huagongshe.com/reaction/992994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18408502 | HCID 18408502 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67526446 | HCID 67526446 | — |
Reaction Steps
THF (5 mL) was added to sodium hydride (55% dispersion in mineral oil, 162 mg) under an argon atmosphere, and a solution of ethyl diethylphosphonoacetate (832 mg) in THF (2 mL) was added dropwise to the mixture at −10° C. After 30 minutes, a solution of 2-(3,4,5-trimethoxyphenyl)thiazole-4-carboaldehyde (942 mg) in THF (8 mL) was slowly added to the resultant mixture, and the mixture was warmed to room temperature over 30 minutes and then stirred for 2 hours. The reaction mixture was diluted with ethyl acetate, washed with a saturated aqueous solution of sodium hydrogencarbonate, water and saturated brine, dried over anhydrous sodium sulfate. After concentrating the reaction mixture under reduced pressure, the resultant crude crystals were recrystallized from ethyl acetate-hexane to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472386B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-c6c4e6e2674e4360b7613ad5213f3c47 |
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| Source note | uspto-grants-2002_10 |
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