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Trifluoroacetic acid → 4-tert-Butyl-3-(2-methoxyethoxy)phenol

HRID 1350862
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HRID 1350862 반응식
C(=O)([O:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])=[C:10]([O:18][CH2:19][CH2:20][O:21][CH3:22])[CH:9]=1)OC(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[C:14]([C:11]1[CH:12]=[CH:13][C:8]([OH:7])=[CH:9][C:10]=1[O:18][CH2:19][CH2:20][O:21][CH3:22])([CH3:17])([CH3:15])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 21097537tert-Butyl 4-tert-butyl-3-(2-methoxyethoxy)phenyl carbonate

생성물 1

HCID 210974934-tert-Butyl-3-(2-methoxyethoxy)phenol수율 59.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a methylene dichloride (3 ml) solution of tert-butyl 4-tert-butyl-3-(2-methoxyethoxy)phenyl carbonate (792 mg, 2.4 mmol) was added trifluoroacetic acid (TFA) (3 ml) and the mixture was stirred for 1 hour at ambient temperature. The solvent was removed under reduced pressure to give a residue, which was applied to a silica gel chromatography column and eluted with ethyl acetate/hexane=⅓ to furnish 0.32 g (59% yield) of the title compound as a white solid.

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후처리

  1. customThe solvent was removed under reduced pressure
  2. customto give a residue, which
  3. washeluted with ethyl acetate/hexane=⅓

출처 및 근거

ORD 기록
ord-b21c5f9208ff468dae39e6e4a163b1d5
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214824B2

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