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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486102Generated: October 28, 2026

N-Isopropylhydroxylamine Hydrochloride → HCID 53808329, compound

https://huagongshe.com/reaction/486102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Isopropylhydroxylamine HydrochlorideHCID 170873—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53858627HCID 53858627—
SolventEthanolHCID 702—
ProductHCID 53808329HCID 5380832998.6%

Reaction Steps

A mixture of N-isopropylhydroxylamine hydrochloride (5.5 g, 0.049 mole), potassium-t-butoxide (4.83 g, 0.043 mole), and ethanol (500 mL) is stirred at room temperature for 15 minutes. 5-[(3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl)methylene]-2-(methylthio)-4(5H)-thiazolone (7.27 g, 0.02 mole) is then added and the mixture is refluxed with stirring for six hours. After removal of the solvent under reduced pressure, the cooled reaction mixture is poured into a mixture of ice-water containing 1N hydrochloric acid and extracted with ether. The organic layer is washed with water, dried, and the solvent is evaporated to give 7.7 g of a residue. The residue is flash chromatographed on silica gel (202 g), eluting first with methylene chloride and then with methylene chloride-methanol (9:1) to give 7.0 purified product. It is recrystallized from methylene chloride-ethyl acetate-ether to give 4.2 g (54%) of pure 5-[[3,5-Bis-(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-2-]hydroxy(1-methylethyl)amino]-4(5 H)-thiazolidinone, (Z)-, mp 208° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290800
Source datasetuspto-grants-1994_03
ORD IDord-110622d8e5784d39a3d4d9ce932c50da
Source noteuspto-grants-1994_03