HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentane, 3-(bromomethyl)- → Dimethyl 5-(2-ethylbutoxyl)isophthalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentane, 3-(bromomethyl)- | HCID 77432 | — |
| Reactant | 1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl ester | HCID 83065 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Dimethyl 5-(2-ethylbutoxyl)isophthalate | HCID 117704493 | — |
Reaction Steps
Dimethyl 5-hydroxyisophthalate (0.44 g, 2.10 mmol) cesium carbonate (1.37 g, 4.20 mmol) and CH3CN (20 mL) were added to a round-bottom flask and stirred for 15-30 min. 3-(Bromomethyl)pentane (0.42 g, 2.52 mmol) was added and the reaction was stirred for 16 h. The solvent was removed under reduced pressure and the reaction mixture was partitioned between EtOAc (50 mL) and H2O (50 mL). The layers were separated and the aqueous layer was extracted with EtOAc (50 mL). The combined organics were dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the desired product which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09439433B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-70fc3e9a7f11415ca319a2dbe0c30442 |
| Source note | uspto-grants-2016_09 |