HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Allylbenzoin methyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Methyl Benzoin | HCID 98097 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Allylbenzoin methyl ether | HCID 129713885 | 83.6% |
Reaction Steps
Benzoin methyl ether (50 g) and t-butanol (500 g) were added to a 1 liter, 3neck, round bottom flask equipped with magnetic stirrer, and placed in an oil bath at 80° C. To this mixture, 33.7 g of potassium t-butoxide was added and the solution stirred for 15 minutes. Allyl Bromide (42.3 g) was added dropwise over a 1 hour period and stirring was continued at 85° C. for 2 more hours then cooled to room temperature. After evaporation of t-butanol and filtration of potassium bromide, the product was distilled at 125° C.±2° C. and 0.05 mgHg to yield 49.2 g of allylbenzoin methyl ether which crystallized upon cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477326 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-650d528e031f4234b82592ce16ae5e53 |
| Source note | uspto-grants-1984_10 |