HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(Phenylmethoxy)-2-(2-propen-1-yl)-1-(2-propen-1-yloxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 18701949 | HCID 18701949 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-(Phenylmethoxy)-2-(2-propen-1-yl)-1-(2-propen-1-yloxy)benzene | HCID 22261130 | — |
Reaction Steps
A mixture of 2-allyl-4-benzyloxy-phenol (ER2-YYR-17) (35.56 g, 148 mmol), allyl bromide (21.5 g, 178 mmol), cesium carbonate (58 g, 178 mmol) and methyl ethyl ketone (400 mL) was refluxed with stirring in a 1 L round bottomed flask. After 23 h, the reaction was cooled and concentrated. The residue was partitioned between water (500 mL) and EtOAc (400 mL). The organic layer was dried (MgSO4) and concentrated to a tan oil, 39.37 (95%) ER0-LKW-190A: 1H NMR (CDCl3) δ 3.45 (dd, 2H), 4.54 (dd, 2H), 5.04 (s, 2H), 5.18 (m, 2H), 5.29 (dd, 1H), 5.46 (dd, 1H), 5.94-6.18 (m, 2H), 6.81 (s, 2H), 6.88 (s, 1H), 7.30-7.48 (m, 5H), MS (ES) m/e 281 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351728B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-dd18b56d31a045fd98dbd5d441db7e2a |
| Source note | uspto-grants-2008_04 |