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[C:1]([C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[C:7]([C:13]([CH3:16])([CH3:15])[CH3:14])[C:6]=1[OH:17])([CH3:4])(C)C.S(=O)(=O)(O)O.COC[O:26][CH3:27]>>[CH2:1]([C:4]1[CH:1]=[C:5]([CH2:10][CH3:9])[CH:6]=[C:7]([C:13]([CH3:16])([CH3:15])[CH3:14])[C:27]=1[OH:26])[C:5]1[CH:10]=[C:9]([CH2:11][CH3:12])[CH:8]=[C:7]([C:13]([CH3:14])([CH3:15])[CH3:16])[C:6]=1[OH:17]참가 물질
4
실험 절차
Into the reactor described in Example 1 hereinbefore there are charged 58.5 g (0.25 g-mol) of 2,6-ditert.butyl4-ethylphenol, 1 g of a concentrated sulfuric acid and 19 g (0.25 g-mol) of methylal are added into the reactor at the temperature of 130° C. over 30 minutes. The reaction mass is treated and 26.2 g of 2,2'-methylene-bis-(4-ethyl-6-tert.butylphenol) are thus obtained which corresponds to 98.9% of the theoretical yield calculated for the reacted 2,6-ditert.butyl-4-ethylphenol (conversion of the latter is 57.5).
후처리
- additionare added into the reactor at the temperature of 130° C. over 30 minutes
- additionThe reaction mass is treated
출처 및 근거
- ORD 기록
- ord-3e385589a73b4152a7eb5968c742ba9d
- 출처 데이터셋
- uspto-grants-1982_03
- 특허 번호
- US04319052
연결된 노트
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