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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119164Generated: November 3, 2026

Ethyl chloroformate → HCID 13689592, compound

https://huagongshe.com/reaction/2119164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20191100HCID 20191100—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13689592HCID 1368959260%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04683234
Source datasetuspto-grants-1987_07
ORD IDord-959dd86657c84975ac0ec7fc174a90db
Source noteuspto-grants-1987_07