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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257041Generated: October 26, 2026

Sodium Hydroxide → 6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-one

https://huagongshe.com/reaction/257041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant6-methoxy-3,4-dihydroisoquinolin-1(2H)-oneHCID 10607392—
SolventDichloromethaneHCID 6344—
Product6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 15908314—

Reaction Steps

To a solution of 6-methoxy-1-oxo-1,2,3,4-tetrahydroisoquinoline (31.3 g, 177 mmol) in CH2Cl2 (300 mL) at -78° is added BBr3 (33.4 mL, 353 mmol). The reaction mixture is allowed to come to ambient temperature and is stirred for 12 hours. After this time the reaction mixture is cooled to 0° and is subsequently neutralized with 5N NaOH (150 mL) solution and saturated NaHCO3 solution. The resulting precipitate is extracted with hot acetone (4×500 mL) and the combined organics are concentrated in vacuo to give 6-hydroxy-1-oxo-1,2,3,4-tetrahydroisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260316
Source datasetuspto-grants-1993_11
ORD IDord-cde0f9c9426944b1bad9653365145d00
Source noteuspto-grants-1993_11