HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → HCID 59135186, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 66716980 | HCID 66716980 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | HCID 59135186 | HCID 59135186 | — |
Reaction Steps
Bromine (80.6 mg, 26 μL, 0.504 mmol) was added to a solution of 2-fluoro-1-isopropyl-3,4-dimethoxybenzene (50.0 mg, 0.252 mmol) and potassium acetate (49.5 mg, 0.504 mmol) in acetic acid (1 mL) at room temperature and the reaction was stirred overnight. The reaction was diluted with water (10 mL) and saturated Na2SO3 (10 mL), then extracted with EtOAc (3×20 mL). The combined extracts were washed with saturated NaHCO3 (2×10 mL), dried (MgSO4) and concentrated in vacuo to afford 1-bromo-3-fluoro-2-isopropyl-4,5-dimethoxybenzene. 1H NMR (600 MHz, CDCl3) δ 6.86 (d, J=2.0 Hz, 1H), 3.87 (s, 3H), 3.81 (s, 3H), 3.43-3.34 (m, 1H), 1.31-1.29 (dd, J=7.1, 1.4 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652049B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-ff66e90677274cce96e78ea9af6a5179 |
| Source note | uspto-grants-2010_01 |