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Methanol → HCID 10893325, 화합물

HRID 2279685
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HRID 2279685 반응식
[CH2:1]([CH:9]1[O:11][CH:10]1[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH3:23][OH:24]>>[OH:11][CH:9]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH:10]([O:24][CH3:23])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 887MethanolHCID 543923Methyl 9,10-epoxyoctadecanoate

생성물 1

HCID 10893325HCID 10893325, 화합물

실험 절차

The methyl 8-(3-octyloxiran-2-yl)octanoate (2) (4.8 g; 0.015 mol), Amberlyst 15 (0.05 g) and methanol in excess (100 mL) were placed under reflux for 12 hours. The reaction mixture was filtered and the methanol removed using a rotary evaporator. The reaction mixture was dissolved in dichloromethane (100 mL) and washed with water (3×50 mL). The dichloromethane solution was separated and evaporated to obtain the intermediate compound 3.

후처리

  1. temperatureunder reflux for 12 hours
  2. filtrationThe reaction mixture was filtered
  3. customthe methanol removed
  4. customa rotary evaporator
  5. dissolutionThe reaction mixture was dissolved in dichloromethane (100 mL)
  6. washwashed with water (3×50 mL)
custom
The dichloromethane solution was separated
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-63b76da5d46d458780dd1683e0c6a92a
    출처 데이터셋
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09133305B2

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