tert-Butyl hydroperoxide → HCID 20367911, 화합물
반응식
[C:1]([N:5]=[N:6][C:7](Cl)([CH2:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH3:8])([CH3:4])([CH3:3])[CH3:2].[C:15]([O:19][OH:20])([CH3:18])([CH3:17])[CH3:16].[OH-].[Na+]>CO>[C:1]([N:5]=[N:6][C:7]([O:20][O:19][C:15]([CH3:18])([CH3:17])[CH3:16])([CH2:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH3:8])([CH3:4])([CH3:3])[CH3:2]참가 물질
5
실험 절차
The 2-t-butylazo-2-(t-butylperoxy)-4,4-dimethylpentane was prepared in 78% crude yield from 3.36 grams (.02moles) of 2-t-butylazo-2-chloro-4,4-dimethylpentane, 2.77 grams (.0277 moles) of 90% t-butyl hydroperoxide and 2.0 grams (.025 moles) of 50% NaOH in 20 ml. of methanol. The procedure was the same as that described in Example X.
출처 및 근거
- ORD 기록
- ord-b5ec473fe6b54fbab4f1327eeba147c5
- 출처 데이터셋
- uspto-grants-1978_02
- 특허 번호
- US04075199
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