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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742646Generated: November 1, 2026

Sodium Chloride → HCID 10387945, compound

https://huagongshe.com/reaction/1742646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10388689HCID 10388689—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 10387945HCID 1038794583.8%

Reaction Steps

After 1.33 g of 2-carboxy-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 numberUS05340807
Source datasetuspto-grants-1994_08
ORD IDord-a7b15e504ad44795b064052550fc6fa7
Source noteuspto-grants-1994_08