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Methanesulfonic Acid → 2-(2-Hydroxy-3-decyl-5-methylphenyl)-2H-benzotriazole

HRID 279960
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인쇄 미리보기

반응식

HRID 279960 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[N:9]1[N:13]=[C:12]2[CH:14]=[CH:15][CH:16]=[CH:17][C:11]2=[N:10]1.CS(O)(=O)=O.[CH2:23]=[CH:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]>>[OH:1][C:2]1[C:7]([CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[N:9]1[N:13]=[C:12]2[CH:14]=[CH:15][CH:16]=[CH:17][C:11]2=[N:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6395Methanesulfonic AcidHCID 133811-Decene2회HCID 17113Drometrizole

생성물 1

HCID 183887892-(2-Hydroxy-3-decyl-5-methylphenyl)-2H-benzotriazole

실험 절차

Using the general procedure of Example 1, 225 grams of 2-(2-hydroxy-5-methylphenyl)-2H-benzotriazole, 65 ml of methanesulfonic acid and 188 ml of 1-decene are heated at 160° C., for a 5-hour period during which time another 564 ml of 1-decene is gradually added to the reaction mixture. The mixture is then cooled and the product isolated by the method described in Example 1 to give 183 grams of the above-named product as a yellow liquid.

후처리

  1. additionis gradually added to the reaction mixture
  • temperatureThe mixture is then cooled
  • customthe product isolated by the method
  • 출처 및 근거

    ORD 기록
    ord-96e056603faf45c48d354f313972abfa
    출처 데이터셋
    uspto-grants-1986_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04587346

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