HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexamethylenetetramine → 3,4-Dihydro-6,7-dimethoxyisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | Trifluoroacetic acid acetate | HCID 23437676 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,4-Dihydro-6,7-dimethoxyisoquinoline | HCID 30058 | 95% |
Reaction Steps
Acetic acid/trifluoroacetic acid (100 mL) was added to a solution of 2-(3,4-dimethoxyphenyl)ethanamine (20 g, 110.38 mmol, 1.00 equiv) and hexamethylenetetramine (31 g, 221.11 mmol, 2.00 equiv). The resulting solution was heated at reflux for about 5 hours in an oil bath. After adding water (100 mL), the solution was extracted with dichloromethane (3×200 mL), and the organic layers were combined and dried over anhydrous sodium sulfate. Solids were removed by filtration, and the resulting filtrate was concentrated in vacuo to give the title product as a yellow oil (20 g, yield=95%). LC-MS: m/z=192 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524733B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-ee60041f966b45bd8141886f41499c14 |
| Source note | uspto-grants-2013_09 |