HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3,4-Tetrahydroisoquinoline → HCID 86729224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| Reactant | 3-(oxiran-2-ylmethoxy)benzaldehyde | HCID 2774049 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86729224 | HCID 86729224 | 63% |
Reaction Steps
A solution of 3-(oxiran-2-ylmethoxy)benzaldehyde (1.0 g, 5.61 mmol) and 1,2,3,4-tetrahydroisoquinoline (1.49 g, 11.22 mmol) in EtOH (20 mL) was heated at 110° C. for 3 h. The solvent was then removed by concentration and the residue dissolved in ethyl acetate, washed with water and the separated organic layer dried and concentrated. The crude product was purified by column chromatography. (1.1 g, yield 63%.) MS (ESI+) e/z: 312.3 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08906900B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-63c3467fdb3f4ca0929324ac1136a1dd |
| Source note | uspto-grants-2014_12 |