HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119164Generated: November 3, 2026
Ethyl chloroformate → HCID 13689592, compound
https://huagongshe.com/reaction/2119164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20191100 | HCID 20191100 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13689592 | HCID 13689592 | 60% |
Reaction Steps
270 mg (0.82 millimole) of 2,6-Dimethyl-5-cyclopropylmethoxycarbonyl-4-(2-nitrophenyl)-dihydropyrimidine in 4 ml of anhydrous tetrahydrofuran was added to 47 mg (0.98 millimole) of sodium hydride as 50% suspension in oil and stirred at room temperature for 5 minutes. Ethyl chloroformate (120 μl), 1.32 millimole) was added and stirred at room temperature for 30 minutes. The reaction solution was diluted with saturated aqueous NaCl solution and extracted with chloroform. The extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure to remove the solvent. The residue was purified on silica gel by thin layer chromatography (developer:chloroform/acetone 10:1, eluant : chloroform/methanol 4:1) to obtain 196 mg (yield 60%) of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04683234 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-959dd86657c84975ac0ec7fc174a90db |
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| Source note | uspto-grants-1987_07 |
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