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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260585Generated: November 1, 2026

Sodium Chloride → HCID 10387945, compound

https://huagongshe.com/reaction/2260585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10388689HCID 10388689—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 10387945HCID 10387945—

Reaction Steps

After 1.33 g of 2-ocarboxy-6,11-dihydro-N-(2,6-diisopropylphenyl)dibenz[b,e]oxepin-11-carboxamide (Compound 25) obtained in Example 25 was dissolved in 10 ml of tetrahydrofuran, 1.0 ml of triethylamine and 0.39 g of ethyl chloroformate were added to the solution under ice cooling. The mixture was stirred at room temperature for 12 hours. Then 0.57 g of sodium borohydride was slowly added to the reaction mixture under ice cooling. After stirring at room temperature for 6 hours, saturated aqueous sodium chloride solution was added and the mixture was extracted with ethyl acetate. After drying over anhydrous magnesium sulfate, the organic layer was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography [eluent: hexane-ethyl acetate (2:1)]. The crude crystal was recrystallized from ethyl acetate-hexane to obtain 1.08 g of Compound 26 as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478835
Source datasetuspto-grants-1995_12
ORD IDord-cae6ac6c02ec4b108b5bcfe11aad221f
Source noteuspto-grants-1995_12