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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416829Generated: November 2, 2026

Sodium borohydride → HCID 10294562, compound

https://huagongshe.com/reaction/1416829

Reaction equation

Participants

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

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 numberUS05916618
Source datasetuspto-grants-1999_06
ORD IDord-70753b6b426e4725bd5c1037ae4a01c7
Source noteuspto-grants-1999_06