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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156908Generated: October 31, 2026

1-(1-Benzoyloxy-1-methylethyl)-isoquinoline → 1-(Propan-2-yl)isoquinoline

https://huagongshe.com/reaction/1156908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzoyloxy-1-methylethyl)-isoquinolineHCID 2825156—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product1-(Propan-2-yl)isoquinolineHCID 1268253668.1%

Reaction Steps

(a-2-2) Ten grams of 1-(1-benzoyloxy-1-methylethyl)-isoquinoline was dissolved in 100 ml of ethanol, and 2 g of 10% palladium-carbon was dissolved. The mixture was stirred in a stream of hydrogen at room temperature and atmospheric pressure for 24 hours. The reaction mixture was filtered through Celite, and the solvent was distilled off. Distillation under reduced pressure afforded 4.0 g of 1-isopropylisoquinoline. (b) A mixture of 9.4 g of 1-isopropylisoquinoline and 12 g of N-hydroxymethyl dichloroacetamide was dissolved in 94 g of conc. sulfuric acid and 9.5 g of 20% fuming sulfuric acid, and the solution was heated for 3 hours. The reaction mixture was poured into water, made weakly alkaline with an aqueous solution of sodium hydroxide, and extracted with ethyl acetate. The solvent was distilled off, and the residue was recrystallized from ethyl acetate-benzene to afford 20 g of 1-isopropyl-5-dichloroacetylaminomethylisoquinoline having a melting point of 150.7° to 151.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337256
Source datasetuspto-grants-1982_06
ORD IDord-1784e27234ec449abef036ccf6fc2d8a
Source noteuspto-grants-1982_06