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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253779Generated: November 1, 2026

Sodium borohydride → HCID 10294562, compound

https://huagongshe.com/reaction/2253779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53786085HCID 53786085—
SolventMethanolHCID 887—
ProductHCID 10294562HCID 1029456266.3%

Reaction Steps

To a suspension of 4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxymethyleneamino-3-trifluoromethylpyrazole (1.0 g) in methanol (10 ml) stirred at room temperature was added sodium borohydride (0.17 g). After 2 hours an additional 0.17 g of sodium borohydride was added, and another 0.34 g added after 1 hours. One hour later the mixture was poured onto water (80 ml). The combined extracts were dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. The white solid thus obtained was purified by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm-2) with dichloromethane as eluent, to furnish 4-cyano-5-methylamino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole as a white solid (0.6 g), m.p. 200°-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232940
Source datasetuspto-grants-1993_08
ORD IDord-7a6e6ea1a5224bcf8d75598f69b7513f
Source noteuspto-grants-1993_08