HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(5-amino-3,4-dihydroisoquinolin-2(1H)-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Amino-1,2,3,4-tetrahydroisoquinoline | HCID 16217499 | — |
| Product | 1-(5-amino-3,4-dihydroisoquinolin-2(1H)-yl)ethanone | HCID 21271726 | — |
Reaction Steps
A stirred mixture of 5-amino-1,2,3,4-tetrahydroisoquinoline (10.0 g) isopropenyl acetate (7.2 g) and ethyl acetate (150 ml) was heated under reflux for 24 hours. The cooled, filtered solution was evaporated under reduced pressure to a small volume. The residual oil was purified by elution from a silica column with ethyl acetate/methanol mixtures followed by crystallisation from ethyl acetate to give 2-acetyl-5-amino-1,2,3,4-tetrahydroisoquinoline as a white solid 6.6 g, m.p. 107°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04812573 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-a7dac60dbebf4db894de4bc2f0cbd37e |
| Source note | uspto-grants-1989_03 |