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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702988Generated: November 1, 2026

1,2,3,4-Tetrahydroisoquinoline → 2-Acetyl-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1702988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
ReactantAcetic AnhydrideHCID 7918—
Product2-Acetyl-1,2,3,4-tetrahydroisoquinolineHCID 600215—

Reaction Steps

A mixture of 100 g. (0.75 mole) 1,2,3,4-tetrahydroisoquinoline and 150 ml. acetic anhydride was stirred at ambient temperature for 24 hours and then concentrated to dryness at reduced pressure. The residual liquid was dissolved in methylene chloride and solid potassium carbonate was added to neutralize the solution. The excess potassium carbonate was removed by filtration and the filtrate was concentrated to dryness at reduced pressure to afford 2-acetyl-1,2,3,4-tetrahydroisoquinoline as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350698
Source datasetuspto-grants-1982_09
ORD IDord-e14e45dfbe2a405e851c75e5561fb59e
Source noteuspto-grants-1982_09