HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 54045189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 54275119 | HCID 54275119 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54045189 | HCID 54045189 | — |
Reaction Steps
A mixture of methyl-3(3-allyl-4-hydroxyphenyl)propionate (12.3 g), anhydrous potassium carbonate (13.8 g), and allylbromide (8.64 mls) in acetone (300 ml) was stirred at ambient temperature for two days. The reaction mixture was filtered and the residue washed with acetone. The filtrate and washings were combined and evaporated to give methyl-3-(3-allyl-4-allyloxyphenyl)proprionate as a pale yellow oil (14.0 g); NMR: 2.58(2H,t), 2.75(2H,t), 3.31(2H,d), 3.55(3H,s), 4.52(2H,d), 4.95-5.45(4H,m), 5.85-6.11(2H,m), 6.85(1H,d) and 7.0(2H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919793 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-a454eb22c2894d89890c13afb8d287f2 |
| Source note | uspto-grants-1999_07 |