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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597207Generated: October 30, 2026

Dichloromethane → 2-Acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline

https://huagongshe.com/reaction/597207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
ReactantHCID 21447025HCID 21447025—
SolventWaterHCID 962—
Product2-Acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinolineHCID 2144700779.9%

Reaction Steps

A mixture of 122.3 g of 5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline-hydrochloride, 36.1 g of sodium acetate, 81.7 g of acetic anhydride, and 500 ml of methylene chloride is stirred for 1 hour at the boiling point. After cooling, the mixture is combined with 500 ml of water and the organic phase is separated and evaporated to dryness under reduced pressure. 99.5 g of 2-acetyl-5-benzyloxy-1,2,3,4-tetrahydro-6-methoxy-isoquinoline are obtained. m.p. = 94° - 95° C. (ethyl acetate - diisopropyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013663
Source datasetuspto-grants-1977_03
ORD IDord-955f010b617943459fe35ffb7051e9cf
Source noteuspto-grants-1977_03