HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2,6-Dimethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 21584902 | HCID 21584902 | — |
| Product | 2,6-Dimethylphenol | HCID 11335 | — |
| Product | HCID 178467684 | HCID 178467684 | — |
Reaction Steps
Substantially the same reaction as in Examples 1 to 9 was conducted except that various alkenyl halides as shown in Table 5 were employed instead of allyl bromide. PPE-1 was used in Examples 17 and 18. Poly 2,6-dimethyl-1,4-phenylene ether [viscosity (ηsp/c): 0.59 (hereinafter referred to as PPE-4)] was used in Examples 19 to 21. A bifunctional polyphenylene ether obtained by oxidative polymerization of 2,6-dimethylphenol (hereinafter referred to as PPE-5) in the presence of bis (3,5-dimethyl-4-hydroxyphenyl) sulfone as a polyfunctional phenol compound was used in Example 22. Toluene/TMEDA (100 ml +2.5 ml) was used as a solvent instead of THF in Examples 19 and 22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04923932 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-f1339ce3546a47f8ae217a83ce1d331f |
| Source note | uspto-grants-1990_05 |