HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromhydrol → HCID 14716731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromhydrol | HCID 166749 | — |
| Reactant | HCID 54436508 | HCID 54436508 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14716731 | HCID 14716731 | 98% |
Reaction Steps
Into a flask of 50 m were charged 1.84 g (7.4 mmol) of 4-(2-methyloctanoyl) anisole and 35 ml of dried toluene, to which was added 8.68 g of anhydrous aluminum bromide under ice cooling with stirring, and further the stirring was continued at room temperature over a night. Thereafter, the reaction mixture was stirred at 40° C. for 4 hours, cooled to room temperature and poured into 100 ml of ice water. After the extraction with 40 ml of toluene twice, the organic layer was washed with 80 ml of water, dried on magnesium sulfate, filtered, concentrated and distilled under a reduced pressure to obtain 1.70 g (7.3 mmol, yield 98%) of a redish brown and oily (+)-4-(2-methyloctanoyl) phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05137653 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-31761682302749f1a40436eb714e2c60 |
| Source note | uspto-grants-1992_08 |