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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645900Generated: October 31, 2026

Benzyl Bromide → 5-(Benzyloxy)-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/1645900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant5-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 13236663—
SolventEthanolHCID 702—
Product5-(Benzyloxy)-3,4-dihydroisoquinolin-1(2H)-oneHCID 738514281%

Reaction Steps

To a mixture of 2.4 g (14.7 mmol) of 3,4-dihydro-5-hydroxy-1(2H)-isoquinolinone and 2.5 g of cesium carbonate in 30 ml of ethanol was added 2.5 g (15.0 mmol) of benzyl bromide. The mixture was stirred for 18 hours at room temperature. Then an additional 2.5 g of cesium carbonate and 2.5 g of benzyl bromide was added and the mixture was heated under reflux conditions for four hours. The reaction was partitioned between water and ether, the ether layer was filtered (to remove solid), dried (MgSO4), and concentrated. The residue was dissolved in hexane, filtered, concentrated, and the residue was crystallized from ethanol to give 3.01 g (81%) of the desired product; mp 171°-173°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05177075
Source datasetuspto-grants-1993_01
ORD IDord-84df8aaa67cf48a8a7aa8ed3930dc482
Source noteuspto-grants-1993_01