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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758882Generated: October 30, 2026

Potassium Hydroxide → HCID 20532838, compound

https://huagongshe.com/reaction/1758882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
Reactant4-Amino-3-nitrophenyl thiocyanateHCID 104677—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 20532838HCID 2053283867.6%

Reaction Steps

To a stirred mixture of 11.7 g (0.06 mole) of 2-nitro-4-thiocyanoaniline in 500 ml of absolute ethanol under nitrogen there is added 2.5 g (0.06 mole) of sodium borohydride in portions. The mixture is stirred at room temperature for 15 minutes and then refluxed for 15 minutes. The heating mantle is removed and 3.9 g (0.06 mole) of KOH in 25 ml of absolute ethanol is added. The mixture is stirred for 1 minute. A solution of 4.8 g (0.06 mole) of (chloromethyl) cyclopropane in 10 ml of absolute ethanol is added and the mixture is stirred at room temperature for 15 minutes then refluxed for 2 hours. Equal amounts of water and CHCl3 are added until 2 layers are formed. The organic layer is separated, dried (MgSO4), and the solvent removed in vacuo to give 9.1 g of an orange-red solid, m.p. 45°-47°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030990
Source datasetuspto-grants-1982_07
ORD IDord-c14543dd5acc401d9ebb1a9babd7f5d6
Source noteuspto-grants-1982_07