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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266676Generated: October 26, 2026

Water → 1,2-Bis(3-chlorophenyl)hydrazine

https://huagongshe.com/reaction/266676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-3-nitrobenzeneHCID 8489—
ReactantSodium HydroxideHCID 14798—
CatalystZincHCID 23994—
SolventDiethyl EtherHCID 3283—
Product1,2-Bis(3-chlorophenyl)hydrazineHCID 25791968.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 50% NaOH (3 mL) was added 3-chloronitrobenzene (10 g, 64 mM). The suspension was warmed to 60° C. and zinc (9 g, 138 mM) was added. During the addition, the temperature of the reaction mixture was kept between 60° and 80° C. After the addition was complete, a solution of 20% NaOH (18 mL, 90 mM) was added followed by water (30 mL). An additional portion of zinc (12 g, 189 mM) was then added and the resulting mixture was stirred between 75°-80° C. for 2 hours. After cooling to room temperature, the mixture was added to ether (200 mL), stirred, and the liquid was decanted. The solids were then resuspended in ether and the extraction was repeated 3 times. The ether extracts were combined, dried (Na2SO4), and concentrated to give a yellow solid. This was purified by flash column chromatography using CH2Cl2 as elutant which afforded the titled compound as a yellow solid (5.5 g, 68%). NMR (CDCl3): 7.12 (t, J=8 Hz, 2H), 6.80 (m, 4H), 6.67 (dd, J1 =1 Hz, J2 =8 Hz, 2H), 5.66 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652239
Source datasetuspto-grants-1997_07
ORD IDord-849d6f9dce954ca088376be8c11a50e5
Source noteuspto-grants-1997_07