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Ethyl Acetate → 2-(4-Ethynyl-2-methylphenoxy)ethanol

HRID 734788
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HRID 734788 반응식
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[CH3:19][C:20]1[CH:29]=[C:28]([C:30]#[C:31][Si](C)(C)C)[CH:27]=[CH:26][C:21]=1[O:22][CH2:23][CH2:24][OH:25].CCOC(C)=O>C1COCC1>[C:30]([C:28]1[CH:27]=[CH:26][C:21]([O:22][CH2:23][CH2:24][OH:25])=[C:20]([CH3:19])[CH:29]=1)#[CH:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 2724141Tetrabutylammonium FluorideHCID 690546062-(2-Methyl-4-trimethylsilanylethynylphenoxy)ethanol

생성물 1

HCID 575658612-(4-Ethynyl-2-methylphenoxy)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

20.8 g (74.4 mmol) of TBAF was added at RT to a solution of 16.8 g (67.6 mmol) of 2-(2-methyl-4-trimethylsilanylethynylphenoxy)ethanol in 500 mL of THF and the mixture was stirred for 3 hours at RT. The reaction mixture was evaporated down in vacuo and the residue dissolved in EtOAc. The organic phase was washed with water and saturated aqueous NaCl solution, dried over sodium sulfate, and evaporated down in vacuo. The crude product was used in the next reaction step without further purification. Yield: 12.0 g (quant. yield); C11H12O2 (M=176.212); calc.: molpeak (M)+: 176; found: molpeak (M)+: 176; Rf value: 0.24 (silica gel, cyc/EtOAc 2:1).

후처리

  1. customThe reaction mixture was evaporated down in vacuo
  2. dissolutionthe residue dissolved in EtOAc
  3. washThe organic phase was washed with water and saturated aqueous NaCl solution
  4. dry with materialdried over sodium sulfate
  5. customevaporated down in vacuo
  6. customThe crude product was used in the next reaction step without further purification

출처 및 근거

ORD 기록
ord-282c171ba39d4cc6b48268fd8384ae65
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592358B2

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