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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192519Generated: November 1, 2026

Sodium borohydride → HCID 178436715, compound

https://huagongshe.com/reaction/1192519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178436714HCID 178436714—
SolventMethanolHCID 887—
ProductHCID 178436715HCID 178436715—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-{4-chloro-6-[(1E)-3,3-diethyltriaz-1-en-1-yl]-5-ethynyl-3′-fluorobiphenyl-2-yl}ethanone (2.3 g, 6.1 mmol) in methanol (38 mL) at 0° C. was treated with sodium borohydride (0.46 g, 12 mmol) in two portions and stirred at 0° C. for 30 minutes. The reaction mixture was quenched with water at 0° C., poured into saturated sodium bicarbonate (50 mL), and extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated to give the desired product (quantitative). This material was used without further purification. LCMS for C20H22ClFN3O (M+H)+: m/z=374.1; Found: 373.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-afd7184ef69c432e83c55765ca5f9621
Source noteuspto-grants-2014_03