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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638998Generated: November 2, 2026

Benzyl Bromide → HCID 14625296, compound

https://huagongshe.com/reaction/1638998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 2752175HCID 2752175—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14625296HCID 14625296—

Reaction Steps

N-Acetyl-6-hydroxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline quarter-hydrate (14.0 g) was dissolved in methylene chloride (200 ml). Benzyl bromide (22.6 ml) was then added, followed by the addition of a solution of potassium hydroxide (4.62 g) in water (200 ml) and then tetra-n-butylammonium bromide (2.04 g). The resulting mixture was stirred vigorously overnight (16 hours). The organic layer was then separated, washed (H2O), dried (MgSO4) and evaporated. Medium pressure chromatography of the residue on silica (Merck "Art.9385") eluting with methylene chloride containing gradually increasing amounts of methanol (0-10%) gave, after collection and evaporation of appropriate fractions, the title compound as a semi-solid which was recrystallised from ethyl acetate to give the pure title compound, 16.84 g, m.p. 125°-6°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882337
Source datasetuspto-grants-1989_11
ORD IDord-1a8cbc5bf5dd472f9a66148548d7bdd1
Source noteuspto-grants-1989_11