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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616103Generated: October 29, 2026

Hydrochloric Acid → HCID 10657374, compound

https://huagongshe.com/reaction/616103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 10563608HCID 10563608—
SolventChloroformHCID 6212—
ProductHCID 10657374HCID 10657374—

Reaction Steps

1.2 G. of 2-amino-4-(4-chlorophenoxy)-1-nitrobenzene in 3ml. concentrated hydrochloric acid is treated with a solution of 6 g. stannous chloride in 3 ml. concentrated hydrochloric acid. The mixture is heated briefly (about ten minutes) on a steam bath, then cooled and treated with potassium bicarbonate and chloroform. The chloroform layer is removed from the filtered mixture, dried and evaporated. 1,2-diamino-4-(4-chlorophenoxy)benzene is isolated as a gum. 1G. of 1,2-diamino-4-(4-chlorophenoxy)benzene in 20 ml. acetone is treated overnight at room temperature with 2.5 g. methoxy carbonyl isothiocyanate. The mixture is concentrated under vacuum and the residue triturated with methanol. Recrystallization from methanol gives pure 1,2-bis-(3-methoxycarbonyl-2-thioureido)-4-(4-chlorophenoxy)benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072696
Source datasetuspto-grants-1978_02
ORD IDord-6f991493f20e4f3f87e16c7784473abb
Source noteuspto-grants-1978_02