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HCID 13107025, 화합물 → 2,6-Di-tert-butyl-4-(5-methyl-1H-imidazol-4-yl)phenol

HRID 980341
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HRID 980341 반응식
[C:1]([C:5]1[CH:6]=[C:7]([C:16]2[NH:17][C:18](=S)[NH:19][C:20]=2[CH3:21])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2]>[Ni].C(O)C>[C:1]([C:5]1[CH:6]=[C:7]([C:16]2[N:17]=[CH:18][NH:19][C:20]=2[CH3:21])[CH:8]=[C:9]([C:12]([CH3:13])([CH3:14])[CH3:15])[C:10]=1[OH:11])([CH3:2])([CH3:3])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13107025HCID 13107025, 화합물

생성물 1

HCID 159146172,6-Di-tert-butyl-4-(5-methyl-1H-imidazol-4-yl)phenol수율 74.1%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

A mixture of 1.5 g of 4-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-methyl-2-thioxo-4-imidazoline, 0.5 g of a Raney nickel catalyst, and 50 ml of absolute ethanol was refluxed for one hour and after filtering the reaction mixture, the filtrate was concentrated under reduced pressure. The residue was recrystallized from a mixture of cyclohexane and n-hexane to provide 1 g of 4-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-methylimidazole.

후처리

  1. temperaturewas refluxed for one hour
  2. filtrationafter filtering the reaction mixture
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe residue was recrystallized from a mixture of cyclohexane and n-hexane

출처 및 근거

ORD 기록
ord-6f6d2261fb2c4c7bb246a48d46aa6138
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04636516

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