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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196988Generated: November 1, 2026

Thionyl Chloride → HCID 14127189, compound

https://huagongshe.com/reaction/1196988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14127188HCID 14127188—
SolventDichloromethaneHCID 6344—
ProductHCID 14127189HCID 1412718983.4%

Reaction Steps

In this process, 8.0 g of N-(1,1-dimethyl-2-hydroxyethyl)-11-oxo-6,11-dihydrodibenz[b,e]oxepin-2-carboxamide is suspended in 100 ml of methylene chloride. To the suspension is added 3.6 g of thionyl chloride under a nitrogen atmosphere and ice-cooling and the mixture is stirred at room temperature for one hour. To the mixture is added 300 ml of methylene chloride, and the mixture is washed with saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate. The solvent is distilled away under reduced pressure and the residue is purified by column chromatography on silica gel (eluent: hexane:ethyl acetate=2:1 ). The resultant crude product is recrystallized from hexane to obtain 6.3 g of the desired product as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116863
Source datasetuspto-grants-1992_05
ORD IDord-fc942880150d4da4bce8f5a4496d1e6a
Source noteuspto-grants-1992_05