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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741698Generated: October 26, 2026

Allyl bromide → 6-Allyloxy-1,2,3,4-tetrahydroisoquinolin-1-one

https://huagongshe.com/reaction/1741698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 15908314—
SolventAcetoneHCID 180—
Product6-Allyloxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 18963952—

Reaction Steps

To a solution of 6-hydroxy-1-oxo-1,2,3,4-tetrahydroisoquinoline (23.8 g, 146 mmol) in acetone (350 mL) is added K2CO3 (34.6 g, 219 mmol) and allyl bromide (19.3 g, 161 mmol). The reaction mixture is then heated to reflux for 24 hours. After this time the solution is filtered and subsequently concentrated in vacuo. The resulting material is washed with hexanes (1×200 mL) and Et2O (1×100 mL) to give 6-allyloxy-l,2,3,4-tetrahydroisoquinolin-1-one as a tan solid, m.p. 105°-107°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334600
Source datasetuspto-grants-1994_08
ORD IDord-6eef9b6eb70040f2b985b7db45fbc591
Source noteuspto-grants-1994_08