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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → Methyl 9,10-epoxyoctadecanoate

HRID 2279684
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HRID 2279684 반응식
[C:1]([O:20][CH3:21])(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].ClC1C=CC=C(C(OO)=[O:30])C=1>ClCCl>[CH2:11]([CH:10]1[O:30][CH:9]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:1]([O:20][CH3:21])=[O:19])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 5364509Methyl Oleate

생성물 1

HCID 543923Methyl 9,10-epoxyoctadecanoate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Methyl oleate (1) (5.0 g; 0.017 mol) (89%) (ITERG) and meta-chloroperbenzoic acid (mCPBA) (4.3 g; 0.025 mol) (Aldrich) were dissolved in dichloromethane (J. T. Baker) (100 mL) and the reaction mixture was mixed under agitation at ambient temperature for 5 hours. The reaction mixture was then filtered and the collected solution was washed with saturated aqueous sodium bicarbonate (3×50 mL) (Aldrich) then with water (3×50 mL). The organic layer was separated and dried over anhydrous sodium sulfate. Finally, the solvent was removed by evaporation under rotation to obtain the intermediate compound 2.

후처리

  1. additionthe reaction mixture was mixed under agitation at ambient temperature for 5 hours
  2. filtrationThe reaction mixture was then filtered
  3. washthe collected solution was washed with saturated aqueous sodium bicarbonate (3×50 mL) (Aldrich)
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous sodium sulfate
  6. customFinally, the solvent was removed by evaporation under rotation

출처 및 근거

ORD 기록
ord-e535bc0e18e74cdbaa96dd3b6bc4c323
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133305B2

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