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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397939Generated: October 28, 2026

1,2,3,4-Tetrahydroisoquinoline → HCID 39866, compound

https://huagongshe.com/reaction/2397939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
ReactantPotassium BicarbonateHCID 516893—
Reactant2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-amineHCID 14171269—
SolventBenzeneHCID 241—
ProductHCID 39866HCID 39866—

Reaction Steps

5-Amino-2-methyl-1,2,3,4-tetrahydroisoquinoline (5.0 g) prepared as in Example 4 was dissolved in dry benzene (75 ml) and 0.5 g of dry potassium bicarbonate was added. A 0.1 mole excess of 2-fluorobenzoyl chloride was dissolved in dry benzene (75 ml) and this solution was added to the solution of the tetrahydroisoquinoline. A white precipitate formed immediately. The mixture was refluxed for 1 hour to insure that the reaction had gone to completion. The precipitate was collected by vacuum filtration and washed with 10% sodium carbonate solution followed by water. The washings were discarded and the remaining residue was recrystallized from ethyl acetate to yield 6.8 g of the desired product as white crystals, m.p. 112°-112.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022900
Source datasetuspto-grants-1977_05
ORD IDord-476796b07cd948a5b1d8e2d0a94684b9
Source noteuspto-grants-1977_05