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3,5-Di-tert-butylcatechol → 3,5-Di-tert-butyl-1,2-benzoquinone

HRID 225205
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인쇄 미리보기

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HRID 225205 반응식
[C:1]([C:5]1[CH:11]=[C:10]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH:9]=[C:7]([OH:8])[C:6]=1[OH:16])([CH3:4])([CH3:3])[CH3:2]>[Ag]=O.CCOCC>[C:1]([C:5]1[C:6](=[O:16])[C:7](=[O:8])[CH:9]=[C:10]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH:11]=1)([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 660993,5-Di-tert-butylcatechol

생성물 1

HCID 769153,5-Di-tert-butyl-1,2-benzoquinone

시약·촉매·용매 2

HCID 92152Silver(II) oxide촉매HCID 3283Diethyl Ether용매

실험 절차

To a solution of 5 g. (22.5 mmol.) of 3,5-di-t-butylcatechol in 75 ml. of ether at 0° was added 25 g. of silver oxide. The reaction mixture was stirred at 0° for 30 minutes then at ambient temperature for an additional 30 minutes. The mixture was filtered and the filtrate was evaporated to dryness. Benzene was added to the residue and the resulting precipitate was collected by filtration and air dried to give 3,5-di-t-butyl-1,2-dioxobenzene, m.p. 110°-112°.

후처리

  1. waitat ambient temperature for an additional 30 minutes
  2. filtrationThe mixture was filtered
  3. customthe filtrate was evaporated to dryness
  4. additionBenzene was added to the residue
  5. filtrationthe resulting precipitate was collected by filtration and air
  6. customdried

출처 및 근거

ORD 기록
ord-9e29192a4e5c4bc396343fbfe4430013
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04236001

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