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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975516Generated: November 1, 2026

Sodium borohydride → HCID 10294562, compound

https://huagongshe.com/reaction/975516

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 numberUS05608077
Source datasetuspto-grants-1997_03
ORD IDord-68faad5d4b19493084d258d241dda2bc
Source noteuspto-grants-1997_03