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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361605Generated: October 31, 2026

Sodium borohydride → HCID 588676, compound

https://huagongshe.com/reaction/361605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3,4-Dihydroisoquinolin-1-yl)benzonitrileHCID 53972608—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 588676HCID 58867689.7%

Reaction Steps

A solution of 3.48 g of 4-(3,4-dihydro-isoquinolin-1-yl)-benzonitrile in 90 ml of methanol was cooled to 5° C. while stirring and treated with 1.7 g of sodium borohydride within 30 min. After completion of the addition, the mixture was stirred at 5° C. for a further 30 min. Subsequently, 50 ml of water were slowly added dropwise and the mixture was stirred at room temperature for a further 10 min. The mixture was diluted with water and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated. 3.15 g of crystalline (RS)-4-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-benzonitrile were obtained. Recrystallization of a sample from diisopropyl ether gave colorless crystals of m.p. 94°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866583
Source datasetuspto-grants-1999_02
ORD IDord-bc55606960c04fbaa56f3c902fdc940f
Source noteuspto-grants-1999_02