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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397053Generated: October 30, 2026

Sodium borohydride → 1-(4-Bromophenyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/397053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Bromophenyl)-6-methoxy-3,4-dihydroisoquinoline hydrochlorideHCID 18172461—
SolventMethanolHCID 887—
Product1-(4-Bromophenyl)-6-methoxy-1,2,3,4-tetrahydroisoquinolineHCID 4316138100%

Reaction Steps

Sodium borohydride (0.720 g, 19.0 mmol) was added in small portions to a solution of 1-(4-bromophenyl)-6-methoxy-3,4-dihydroisoquinoline, hydrochloride (3.62 g, 10.2 mmol) in MeOH (30 ml) at 0° C. The reaction mixture was stirred for 30 min, warmed to rt, and stirred at rt for 1 hr, then quenched by the dropwise addition of H2O (10 ml). Acetic acid (10 drops) was added with stirring, and the resulting mixture was basified to pH 10 with 1N NaOH and extracted with EtOAc (3×25 ml). The combined extracts were washed with 1N NaOH followed by saturated NaCl solution, dried over Na2SO4, and concentrated in vacuo to give 3.24 g (100% yield) of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608203B2
Source datasetuspto-grants-2003_08
ORD IDord-87231351aac346acb036eadc66b2b0c2
Source noteuspto-grants-2003_08