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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286021Generated: October 26, 2026

Water → Hydrazine,1,2-bis(2-chlorophenyl)-

https://huagongshe.com/reaction/2286021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1-ButanolHCID 263—
ProductHydrazine,1,2-bis(2-chlorophenyl)-HCID 2050845978.2%

Reaction Steps

630 g o-chloronitrobenzene, 615 g water and 185 g sodium hydroxide (corresponding to a 23.1 wt. % aqueous solution), 0.9 g naphthalenediol-1,4, 535 g n-butanol and 1.0 g palladium on alumina (5% Pd) (the quantitative ratio of palladium metal to o-chloronitrobenzene used being 0.00008:1) are hydrogenated at a hydrogen pressure of 6 bars and at 55° to 65° C. for 4 hours and worked up as described in Example 1. 396 g pure 2,2'-dichlorohydrazobenzene of a purity of better than 98% is obtained in a yield of 78% of theory. In addition, 37 g o-chloroaniline is obtained which after the n-butanol has been drawn off is distillable under vacuum and thus may be recovered pure. When the distillation residue is mixed with 65 g n-butanol of 60° C., a second fraction of 61 g 2,2'-dichlorohydrazobenzene of a purity of from 97 to 98% crystallizes out on cooling. The total hydrazobenzene yield thus is 89.8%. In addition, 7.3 wt. % o-chloroaniline is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04326078
Source datasetuspto-grants-1982_04
ORD IDord-bb279d08371e412898b5d605e4e05456
Source noteuspto-grants-1982_04