HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,6-Trimethylphenol → 4-bromo-2,3,6-trimethyl-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,6-Trimethylphenol | HCID 17016 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-2,3,6-trimethyl-phenol | HCID 10822548 | — |
Reaction Steps
10 g (71 mmol) of 2,3,6-trimethylphenol are initially introduced in a solvent mixture consisting of 250 ml of dichloromethane and 190 ml of methanol, and 35.4 g (72 mmol) of tetrabutylammonium tribromide in 170 ml of dichloromethane and 130 ml of methanol are added. After 5 h at room temperature, the batch is evaporated in a rotary evaporator, and the residue remaining is taken up in MTB. The organic solution is washed three times with water, dried over sodium sulfate and evaporated in a rotary evaporator. The crystalline residue obtained is employed in the next step without further work-up.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296948B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-129b732a4dfa4faebd04e3e20bcbb174 |
| Source note | uspto-grants-2016_03 |