HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600891Generated: October 30, 2026
Hydrochloric Acid → HCID 86591641, compound
https://huagongshe.com/reaction/600891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (Diethoxyphosphinyl)acetic acid | HCID 36704 | — |
| Reactant | HCID 11346406 | HCID 11346406 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86591641 | HCID 86591641 | 70% |
Reaction Steps
Diethylphosphonoacetic acid (32.8 g, 166 mmol) was dissolved in anhydrous benzene (700 ml), and after adding N,N′-dimethylformamide (1 ml, thionyl chloride (18.2 ml, 250 mmol) was added thereto and heated under reflux for 1.5 hours. After letting the reaction solution cool, it was concentrated under a reduced pressure, and after adding dried toluene (100 ml) thereto, its concentration under a reduced pressure was performed again. After repeating this operation 3 times, the concentrate was dissolved in anhydrous tetrahydrofuran (300 ml) and after adding dropwise an anhydrous tetrahydrofuran (300 ml) solution of ethyl 1-[2-[N-[1-(S)-phenylethyl]amino]acetyl]cyclopropanecarboxylate (45.7 g, 166 mmol) and triethylamine (25.1 ml, 183 mmol) while stirring and cooling with ice, it was stirred while cooling with ice for 1.5 hours and then stirred at room temperature for 2 hours. After adding 1 mol/l hydrochloric acid (300 ml) and ethyl acetate (300 ml) to the reaction solution and performing an extraction operation, the organic layer was separated. The aqueous layer was then subjected to extraction with ethyl acetate (300 ml) and the combined organic layer was washed with saturated sodium bicarbonate water (300 ml) and saturated saline solution (300 ml) in that order, and then dried over anhydrous sodium sulfate. After filtering and then concentrating the filtrate under a reduced pressure, 43.6 g (70%) of the title compound was obtained as a yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902226B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-fd3a283c69734419b9ac3eba8a948814 |
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| Source note | uspto-grants-2011_03 |
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