HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Bromo-2-cyclohexyl-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | o-Cyclohexylphenol | HCID 8396 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-2-cyclohexyl-phenol | HCID 22134516 | 93% |
Reaction Steps
To a stirring solution of 2-cyclohexylphenol (26.0 g, 146.8 mmol) in glacial acetic acid (100 mL) was added HBr in acetic acid (150 mL of 33% w/w,) and H2O (52 mL), followed by the dropwise addition of DMSO (100 mL) over 10 min. The reaction was then carefully quenched with saturated NaHCO3 and concentrated in vacuo. The residue was brought up in ether (400 mL), washed with water (2×100 mL) and brine (1×100 mL), and dried over anhydrous Na2SO4, filtered and concentration to yield a crude oil that was purified by silica gel column chromatography, using 15-30% EtOAc/hexane gradient to yield 4-bromo-2-cyclohexyl-phenol (35.0 g, 93%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354427B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-6033354e184d409392dfbeab50f88415 |
| Source note | uspto-grants-2013_01 |