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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 53875204, 화합물

HRID 1076746
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HRID 1076746 반응식
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH:11]([CH3:18])[CH2:12][CH2:13][CH2:14][CH:15]([CH3:17])[CH3:16])=[CH:6][CH:5]=1.O>C1C=CC=CC=1>[CH3:18][CH:11]([O:10][C:7]1[CH:8]=[CH:9][C:4]([CH2:3][OH:2])=[CH:5][CH:6]=1)[CH2:12][CH2:13][CH2:14][CH:15]([CH3:16])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 54404637HCID 54404637, 화합물

생성물 1

HCID 53875204HCID 53875204, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

42 g of p-[(1,5-dimethylhexyl)oxy]benzoic acid methyl ester is dissolved in 250 ml of benzene and, with stirring, treated dropwise with 50 g of 70% bis(2-methoxy-ethoxy)sodium aluminum hydride. The reaction solution is further stirred at 25°C. for 5 hours and thereafter treated with water. The organic phase is separated off, dried under sodium sulfate, carefully filtered (using a filter aid) and evaporated under reduced pressure. There is obtained a residual of p-[(1,5-dimethylhexyl)oxy]benzyl alcohol; B.P. 180°-182°C/1.0 mmHg.

후처리

  1. stirring
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The reaction solution is further stirred at 25°C. for 5 hours
  • customThe organic phase is separated off
  • customdried under sodium sulfate
  • filtrationcarefully filtered (
  • customevaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-b9236b18024f4024a793dca661e42593
    출처 데이터셋
    uspto-grants-1976_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03957833

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