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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methylhydroquinone → Durohydroquinone

HRID 380780
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인쇄 미리보기

반응식

HRID 380780 반응식
[CH3:1]C1C=C(O)C=CC=1O.[O-2].[La+3].[O-2].[O-2].[La+3].CC1C(C)=C(C=CC=1O)O.[CH3:25][C:26]1[C:27]([OH:35])=[C:28]([CH3:34])[C:29]([CH3:33])=[C:30]([CH:32]=1)[OH:31]>CO>[CH3:25][C:26]1[C:27]([OH:35])=[C:28]([CH3:34])[C:29]([CH3:33])=[C:30]([OH:31])[C:32]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7253Methylhydroquinone2회HCID 12785TrimethylhydroquinoneHCID 691002,3-DimethylhydroquinoneHCID 150906Lanthanum sesquioxide

생성물 1

HCID 136346Durohydroquinone

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Into an autoclave (inner volume: 9 ml, made of SUS 316, equipped with a manometer) were charged 0.098 g of methylhydroquinone, 3.491 g of methanol and 7 mg of lanthanum oxide (manufactured by High Purity Chemicals Co.). The reaction was started by elevating the temperature up to 350° C. with sand bath. The pressure during the reaction was 18 MPa. After 2 hours, the autoclave was quickly cooled and the reaction solution was taken out from the autoclave when the temperature was cooled back to the room temperature. The measurement according to the process described above revealed that the conversion of methylhydroquinone was 32% by mole, the selectivity of dimethylhydroquinone was 80% by mole, the selectivity of trimethylhydroquinone was 10% by mole and no tetramethylhydroquinone was produced.

후처리

  1. customequipped with a manometer)
  2. customup to 350° C.
  3. temperaturethe autoclave was quickly cooled

출처 및 근거

ORD 기록
ord-67e836e63e8a45298e2acbd8917caeef
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06303801B1

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