Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840725Generated: October 31, 2026

Ethanol → [4-(4-Chlorophenoxy)-3-nitrophenyl]hydrazine

https://huagongshe.com/reaction/840725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantStannous chloride dihydrateHCID 61436—
Reactant4-(4-Chlorophenoxy)-3-nitroanilineHCID 15580149—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product[4-(4-Chlorophenoxy)-3-nitrophenyl]hydrazineHCID 22620231—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.52 g of sodium nitrite in 5 ml of water was added dropwise to a stirred mixture consisting of 1.9 g of 4-(4-chlorophenoxy)-3-nitroaniline, 25 ml of concentrated hydrochloric acid and 25 ml of ethanol cooled to 0° C., and the mixture was then stirred at 0° C. for 60 min and subsequently added dropwise to a suspension of 8.5 g of tin dichloride dihydrate in 8 ml of concentrated HCl. The precipitate was filtered off with suction, washed with water, suspended in 200 ml of water under nitrogen and decomposed with 100 ml of 30% strength sodium hydroxide solution at 10-15° C. The oil formed was extracted by shaking with ethyl acetate and washed with water, and the organic phase was dried with sodium sulfate. The product was then precipitated with isopropanolic HCl, filtered off with suction and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369088B2
Source datasetuspto-grants-2002_04
ORD IDord-5facb5f62df24784972b9e1daea401d9
Source noteuspto-grants-2002_04