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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032679Generated: October 31, 2026

Thionyl Chloride → HCID 19915720, compound

https://huagongshe.com/reaction/1032679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 19915728HCID 19915728—
ProductHCID 19915720HCID 19915720—

Reaction Steps

Thionyl chloride (50 ml) was added dropwise with stirring and cooling in an ice/water bath to 1-(N-methyl-N-(4-nitrophenethyl)amino)-2-hydroxypropane (1.5 g). After stirring at room temperature for 1 hour, the solution was refluxed on a steam bath for a further 2 hours. The solution was evaporated to dryness and the residual oil partitioned between 2N aqueous sodium carbonate solution and ethyl acetate. After two further extractions with ethyl acetate, the organic portions were combined, washed with a saturated brine solution, dried over anhydrous magnesium sulphate, filtered and evaporated to dryness. The resultant brown oil was chromatographed on silica ("Kieselgel 60"- Trade Mark) eluting with ethyl acetate followed by collection and evaporation of suitable fractions to give the title compound as a yellow oil, (0.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959366
Source datasetuspto-grants-1990_09
ORD IDord-2e8030a2e31343fd9366e264a728af7d
Source noteuspto-grants-1990_09