HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-allyloxy-4-fluoro-benzoic Acid Ethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-fluoro-3-hydroxybenzoate | HCID 18007712 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-allyloxy-4-fluoro-benzoic Acid Ethyl Ester | HCID 66998735 | — |
Reaction Steps
K2CO3 (96.9 mmol) and 3-bromo-1-propen (64.6 mmol) are added to a solution of 4-fluoro-3-hydroxy-benzoic acid ethyl ester (32.3 mmol) in acetone (50 mL). The mixture is heated to reflux for 16 h, filtered and cooled to RT. The solvents are removed in vacuo to give the desired product which is used without further purification. LC-MS: tR=1.01 min; [M+CH3CN+H]+=266.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063099B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b0f29086079d4af2aca10cfe0353505d |
| Source note | uspto-grants-2011_11 |