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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650262Generated: October 30, 2026

Allyl bromide → 2,6-Dimethylphenol

https://huagongshe.com/reaction/1650262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 21584902HCID 21584902—
Product2,6-DimethylphenolHCID 11335—
ProductHCID 178467684HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923932
Source datasetuspto-grants-1990_05
ORD IDord-f1339ce3546a47f8ae217a83ce1d331f
Source noteuspto-grants-1990_05