HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 8-Bromo2-dipropylamino-3,4-dihydronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | 8-Bromo-1,2,3,4-tetrahydronaphthalen-2-one | HCID 4136187 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 8-Bromo2-dipropylamino-3,4-dihydronaphthalene | HCID 19043207 | — |
Reaction Steps
To a solution of 8-bromo-2-tetralone (3.0 gm, 13.3 mMol) in toluene (25 mL) were added di-n-propylamine (3.5 mL, 26 mMol) and p-toluenesulfonic acid (100 mg, 0.52 mMol). The reaction was heated to reflux, water being collected in a Dean-Stark trap. After four hours the reaction was concentrated in vacuo to give 8-bromo-2-dipropylamino-3,4-dihydronaphthalene as a dark liquid which was immediately dissolved in methanol (50 mL) and acetic acid (5 mL). To this solution was then added sodium borohydride (2.0 gm, 52.9 mMol), and the mixture was stirred 18 hours at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05258379 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-c4c4d1d7dee4450397d8dd5c3042dd8b |
| Source note | uspto-grants-1993_11 |