HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-(Prop-2-en-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Prop-2-en-1-yl)benzaldehyde | HCID 22022690 | 101.3% |
Reaction Steps
The ethylene acetal of 3-bromobenzaldehyde (10 g) is converted into the Grignard reagent by reaction with magnesium (1.13 g) in dry THF (ca. 250 ml). Cuprous bromide (0.9 g) is added and the mixture is cooled in cardice. Allylbromide (8.52 g) in dry THF is then added and the mixture is stirred overnight following which saturated ammonium chloride is added, the mixture is extracted with diethyl ether (3 times), the ether extract is washed, dried and the solvent evaporated to yield the crude ethylene acetal of 3-allylbenzaldehyde (8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515808 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-6aae9a641d6640b5a687d8b7d3b7c259 |
| Source note | uspto-grants-1985_05 |