Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963983Generated: October 30, 2026

Sodium borohydride → 2-[4,4-Bis-(4-fluorophenyl)butyl]-1,2,3,4-tetrahydroisoquinolin-5-ol

https://huagongshe.com/reaction/963983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-[4,4-Bis-(4-fluorophenyl)butyl]-5-hydroxyisoquinolinium bromideHCID 15870891—
SolventMethanolHCID 887—
Product2-[4,4-Bis-(4-fluorophenyl)butyl]-1,2,3,4-tetrahydroisoquinolin-5-olHCID 1587088860.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[4,4-bis-(4-fluorophenyl)butyl]-5-hydroxyisoquinolinium bromide (4.99 g, 10.61 mmol) in 165 mL of methanol at 0° C. was added sodium borohydride (1.54 g, 40.71 mmol). The reaction mixture was stirred at 0° C. for 15 minutes, then at room temperature for 15 minutes. The mixture was concentrated on a rotavap. The residue was dissolved in ethyl acetate (200 mL) and washed with saturated ammonium chloride solution (150 mL). The organic layer was collected, and the aqueous layer was extracted with ethyl acetate (1×100 mL). The combined organic layers was dried with magnesium sulphate, filtered, and concentrated to give 1.9 g of crude product as a brown oil. The oil was chromatographed on silica gel eluted with 50% ethyl acetate in hexanes to give 2.54 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767129
Source datasetuspto-grants-1998_06
ORD IDord-d9f2ac091fd34998a6b866074fb20297
Source noteuspto-grants-1998_06