HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 14147378, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-one | HCID 10943271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14147378 | HCID 14147378 | 98.3% |
Reaction Steps
A mixture of 6-acetyl-7-hydroxy-1,2,3,4-tetrahydronaphthalene (2.0 g), allyl bromide (1.7 g), anhydrous potassium carbonate (2.2 g) and N,N-dimethylformamide (50 ml) was stirred at room temperature for 24 hours. The mixture was then poured into ice/water (400 ml) and stirred. The precipitate was filtered off, washed with water and then dried to leave, as an off-white powder, 6-acetyl-7-allyloxy-1,2,3,4-tetrahydronaphthalene (2.38 g), mp 62°-63°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04159273 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-204a06a8452e4c6f857cf73276767f8f |
| Source note | uspto-grants-1979_06 |