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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166372Generated: October 31, 2026

1,2,3,4-Tetrahydroisoquinoline → HCID 14405661, compound

https://huagongshe.com/reaction/2166372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
ReactantEthyl 1-benzylpiperidine-4-carboxylateHCID 90423—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 14405661HCID 1440566190.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

251 ml (594 mmol) of trimethylaluminium (at a concentration of 25% in hexane) are introduced under an argon atmosphere into 400 ml of toluene. The solution is cooled in an ice bath and 81.5 g (612 mmol) of 1,2,3,4-tetrahydroisoquinoline, dissolved in 200 ml of toluene, are added. The mixture is heated to approximately 50° C. and 95 g (384 mmol) of ethyl 1-phenylmethyl-4-piperidinecarboxylate, dissolved in 400 ml of toluene, are added. The mixture is heated under reflux for 2 h, approximately 250 ml of solvent being removed by means of a Dean and Stark apparatus. The mixture is cooled in an ice bath and hydrolysed by slowly adding 250 ml of water, and the insoluble material is filtered off, it being rinsed with ethyl acetate. The filtrate is washed three times with water, the organic phase dried over sodium sulphate, the solvent evaporated off and the residue recrystallized in cyclohexane. 116.6 g of product are obtained. Melting point: 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945096
Source datasetuspto-grants-1990_07
ORD IDord-6abed2abf00847e7bd3d2b47b5f2fdc7
Source noteuspto-grants-1990_07