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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838993Generated: October 30, 2026

Potassium Hydroxide → 4-{[(2,2-Dichlorocyclopropyl)methyl]sulfanyl}-2-nitroaniline

https://huagongshe.com/reaction/838993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-Amino-3-nitrophenyl thiocyanateHCID 104677—
ReactantSodium borohydrideHCID 4311764—
Reactant2-BROMOMETHYL-1 1-DICHLOROCYCLOPROPANEHCID 4739582—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product4-{[(2,2-Dichlorocyclopropyl)methyl]sulfanyl}-2-nitroanilineHCID 2053283954.6%

Reaction Steps

To a stirred mixture of 11.75 g (0.06 mole) of 2-nitro-4-thiocyanoaniline in 500 ml of absolute ethanol under N2 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 30 ml of absolute ethanol is added. The mixture is stirred for 1 minute. A solution of 12.25 g (0.06 mole) of 1-bromomethyl-2,2-dichlorocyclopropane in 30 ml of absolute ethanol is added and the mixture is stirred at room temperature for 15 minutes and then refluxed for 2 hours. Equal amounts of H2O and CHCl3 are added until 2 layers are formed. The organic layer is separated, dried (MgSO4), and the solvent removed in vacuo to give a red oil which is chromatographed on silica gel. Elution with ethyl ether gives 9.6 g of red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093732
Source datasetuspto-grants-1978_06
ORD IDord-cba037499cf64fc2a329aaaa220dee3b
Source noteuspto-grants-1978_06