4-tert-Butylphenol → 4-tert-Butylcatechol

HRID 1605630ノート

反応式

HRID 1605630 の反応式
[O:1](CCCCCCCC)P(OP([O-])([O-])=O)(=O)OCCCCCCCC.[C:26]([C:30]1[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=1)([CH3:29])([CH3:28])[CH3:27]>>[C:26]([C:30]1[CH:35]=[C:34]([OH:1])[C:33](=[CH:32][CH:31]=1)[OH:36])([CH3:29])([CH3:27])[CH3:28]

参加物

3

反応物 2

HCID 73934-tert-ButylphenolHCID 5737108926658-09-3

生成物 1

HCID 73814-tert-Butylcatechol収率 75%

実験手順

The procedure of Example 7 was repeated, except 0.2% by weight of dioctyl pyrophosphate was used in place of Na5R'5 (P3O10)2. Consequently, the conversion of para-tert.-butyl phenol was 7.2%, 4-tert.-butyl pyrocatechol was formed in a yield of 75% based on the converted butyl phenol and the conversion of peracetate was 99.0%.

出典と根拠

ORDレコード
ord-e0d532a5d9434c53ac75e0c0f2d4ff3f
出典データセット
uspto-grants-1976_04
特許番号
US03950437

反応ノート

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