HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-Bromo-2-chloro-6-ethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1-(5-Bromo-3-chloro-2-hydroxyphenyl)ethan-1-one | HCID 24211939 | — |
| Solvent | Triethylene Glycol | HCID 8172 | — |
| Product | 4-Bromo-2-chloro-6-ethylphenol | HCID 58762684 | 83% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
Sodium hydroxide (1.2 g, 30 mmol) and hydrazine monohydrate (1.75 mL, 36 mmol) were added to a solution of 5′-bromo-3′-chloro-2′-hydroxyacetophenone (3 g, 12 mmol) dissolved in triethylene glycol (15 mL). The reaction mixture was heated to 160° C. for 72 hours and then partitioned between 1N HCl and EtOAc. The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated. The residue was purified by flash silica gel chromatography (0% to 10% EtOAc in hexanes) to give the title compound (2.34 g, 83%). 1H NMR (400 MHz, CDCl3): δ 1.22 (t, J=7.6 Hz, 3H), 2.65 (q, J=7.6 Hz, 2H), 5.55 (s, 1H), 7.17 (s, 1H), 7.31 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473790B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-5ba219b2df4d4a9d962d76e6c71051d4 |
| Source note | uspto-grants-2009_01 |