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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601041Generated: November 1, 2026

Methanol → 6-Bromo-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1601041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant6-Bromo-3,4-dihydro-2H-isoquinolin-1-oneHCID 21865450—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-1,2,3,4-tetrahydroisoquinolineHCID 15885183—

Reaction Steps

A solution of 6-bromo-3,4-dihydro-1(1H)-isoquinolinone (Example 31, Step 1; 5.5 g, 1.0 mmol) in THF (25 mL) was treated with 1M BH3 in THF (5 mL, 5 mmol) and heated at reflux for 20 h. To the mixture was added MeOH (5 mL), the solvent removed and the residue heated with 2N HCl for 3 h. The reaction was cooled, made basic with aqueous NH4OH and extracted with CH2Cl2, dried and evaporated to give the title compound as a gum which was used as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977134
Source datasetuspto-grants-1999_11
ORD IDord-35c7fdf93afe41d6a3b417e402592e04
Source noteuspto-grants-1999_11