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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082386Generated: October 31, 2026

Water → HCID 54193382, compound

https://huagongshe.com/reaction/2082386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54054498HCID 54054498—
SolventMethanolHCID 887—
ProductHCID 54193382HCID 54193382—

Reaction Steps

2-(2,6-dichloro-4-trifluoromethylphenyl)-4-[(2-amino-1,2-dicyanoethenylimino)methyl]-2H-1,2,3-triazole (8 g) (prepared as in Example 1) was dissolved in methanol (50 ml) and tetrahydrofuran (75 ml) and then sodium borohydride (0.76 g) was added portionwise. This mixture was stirred for 20 minutes at room temperature and then poured into water to give a brown solid. This was purified by flash column chromatography to give 2-(2,6-dichloro-4-trifluoromethylphenyl)-4-[(2-amino-1,2-dicyanoethenylamino)methyl]-2H-1,2,3-triazole, m.p. 191°-192°. A mixture of this compound (1.8 g), nicotinamide (0.6 g), N-chlorosuccinimide (0.6 g) and dimethylformamide was heated at 65°-70° for 10 minutes. The mixture was poured into water and extracted with diethyl ether. Conventional work-up and purification by flash column chromatography gave 2-(2,6-dichloro-4-trifluoromethylphenyl)-4-(4,5-dicyano-4-imidazolin-2-yl)-2H-1,2,3-triazole, m.p. 219°-220° (dec). (Compound 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189053
Source datasetuspto-grants-1993_02
ORD IDord-85646ee9dd084cd9afdb9eec160ab5b8
Source noteuspto-grants-1993_02