HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196860Generated: November 1, 2026
Diethyl chlorophosphate → HCID 19896721, compound
https://huagongshe.com/reaction/1196860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Tert-butyl-1,2,3,4-tetrahydro-2,3-dioxoquinoxaline | HCID 10608855 | — |
| Reactant | HCID 19896738 | HCID 19896738 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19896721 | HCID 19896721 | — |
Reaction Steps
To a stirred solution of 1-tert-butyl-1,2,3,4-tetrahydro-2,3-dioxoquinoxaline (6.54 g, 30 mmol) in dry dimethylformamide (DMF) (30 ml) under nitrogen was added sodium hydride (80% in oil, 9.6 g, 32 mmol). After stirring for 10 min. the solution was cooled to -20° C. and diethyl chlorophosphate (5.6 ml, 39 mmol) was added. The mixture was allowed to reach room temperature and then cooled to -30° C., whereafter 5-isocyanomethyl-3-methylisoxazole (3.0 g, 25 mmol) and finally a solution of potassium tert-butoxide (3.0 g, 26 mmol) in dry DMF (30 ml) was added keeping the temperature below -20° C. The reaction mixture was warmed to room temperature, acidified with acetic acid (1 ml) and evaporated in vacuo. The residue was triturated with water and ether, and the resulting precipitate was filtered off and partitioned between 0.5 M aqueous sodium hydroxide (50 ml) and dichloromethane (50 ml). The organic layer was filtered through celite, dried, and evaporated to give the title compound, m.p. 395° C. (Compound 17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116841 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-6176151ec8dd45938ad03fa9d82e3ecb |
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| Source note | uspto-grants-1992_05 |
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