HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620722Generated: October 30, 2026
Triethylamine → 4-Diethoxyphosphinylmethylbenzamide
https://huagongshe.com/reaction/620722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-[(Diethoxyphosphoryl)methyl]benzoic acid | HCID 13745801 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Diethoxyphosphinylmethylbenzamide | HCID 13745824 | — |
Reaction Steps
To a solution of 1.36 g of 4-diethoxyphosphinylmethylbenzoic acid and 0.56 g of triethylamine in 15 ml of dry THF was slowly added a solution of 0.60 g of ethyl chlorocarbonate in 2 ml of dry THF under ice-cooling with stirring. After stirring for 30 minutes under ice-cooling, ammonia gas was slowly bubbled into the mixture for 15 minutes, stirred for 2 hours at room temperature. After adding 30 ml of water, the reaction mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and the solvent was evaporated. The residue was subjected to silica gel column chromatography (eluent; chloroform:methanol=10:1) to give 4-diethoxyphosphinylmethylbenzamide. it was recrystallized from chloroform-benzene mixture to give 0.80 g of colorless plate crystals. mp: 177.0°-177.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822780 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-3a81b6bfae85436eb1d9c948349228e3 |
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| Source note | uspto-grants-1989_04 |
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