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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567113Generated: October 29, 2026

Sodium borohydride → 1-(4-Trifluoromethoxyphenyl)-1,2,3,4-tetrahydro-isoquinoline

https://huagongshe.com/reaction/567113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Trifluoromethoxyphenyl)-3,4-dihydro-isoquinolineHCID 21264376—
SolventMethanolHCID 887—
Product1-(4-Trifluoromethoxyphenyl)-1,2,3,4-tetrahydro-isoquinolineHCID 21264406—

Reaction Steps

The above 1-(4-trifluoromethoxyphenyl)-3,4-dihydro-isoquinoline (0.40 g, 1.4 mmol) was dissolved in methanol (20 mL) and sodium borohydride (0.08 g, 2.1 mmol) was added slowly. The reaction mixture was stirred at room temperature for 2.5 hours. The mixture was evaporated in vacuo, redissolved in 1 N NaOH (20 mL) and extracted with dichloromethane (50 mL). The organic phase was dried (MgSO4), filtered and evaporated in vacuo. The remaining oil (0.35 g) was purified by column chromatography on silica gel eluting with a mixture of dichloromethane and methanol (9:1). This afforded 0.56 g (56%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177443B1
Source datasetuspto-grants-2001_01
ORD IDord-3315afc3abdf4e7aac800e6cc6432e12
Source noteuspto-grants-2001_01