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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290262Generated: October 30, 2026

Ammonium Hydroxide → 2-Cyanimino-3-(4-hydroxy-benzyl)-thiazolidine

https://huagongshe.com/reaction/2290262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant{3-[(4-Methoxyphenyl)methyl]-1,3-thiazolidin-2-ylidene}cyanamideHCID 14306204—
SolventDichloromethaneHCID 6344—
Product2-Cyanimino-3-(4-hydroxy-benzyl)-thiazolidineHCID 143062080%

Reaction Steps

0.49 g (2 moles) of 2-cyanimino-3-(4-methoxybenzyl)-thiazolidine are dissolved in 12 ml of dichloromethane and a solution of 3.01 g (1.14 ml, 13 mmoles) of borotribromide in 5 ml of dichloromethane is added in an argon atmosphere, dropwise. The mixture is stirred for 12 hours and is then alkalized with an aqueous ammonium hydroxide solution, under stirring and cooling. The phases are separated and the organic phase is evaporated. 0.22 g of 2-cyanimino-3-(4-hydroxy-benzyl)-thiazolidine are obtained in a white crystalline form, melting at 175° to 177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04616025
Source datasetuspto-grants-1986_10
ORD IDord-381a7baed05e437f92d1bca03ee64567
Source noteuspto-grants-1986_10