HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylphenol → 4-Bromo-2-ethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylphenol | HCID 6997 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Bromo-2-ethylphenol | HCID 87877 | 100.6% |
Reaction Steps
5.57 g (45 mmol) of 2-ethylphenol are placed in 250 ml of chloroform in a round-bottomed flask and under a stream of nitrogen. 43.4 g (90 mmol) of tetrabutylammonium tribromide are added portionwise. The medium is stirred for 1 hour at room temperature and is then hydrolysed with saturated aqueous sodium thiosulfate solution. The organic phase is washed with water, dried over magnesium sulfate, filtered and then evaporated. 9.1 g (100%) of the expected product are obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924400B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-f640c1f96cc744ada21ed968654e5f60 |
| Source note | uspto-grants-2005_08 |