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Triethylsilane → (3,4-Dihydroxyphenyl)(morpholino)methanone

HRID 2103116
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인쇄 미리보기

반응식

HRID 2103116 반응식
C1(C2(C3C=CC=CC=3)[O:11][C:10]3[CH:12]=[CH:13][C:14]([C:16]([N:18]4[CH2:23][CH2:22][O:21][CH2:20][CH2:19]4)=[O:17])=[CH:15][C:9]=3[O:8]2)C=CC=CC=1.C([SiH](CC)CC)C>FC(F)(F)C(O)=O>[OH:8][C:9]1[CH:15]=[C:14]([C:16]([N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)=[O:17])[CH:13]=[CH:12][C:10]=1[OH:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12052TriethylsilaneHCID 10452791(2,2-Diphenylbenzo[d][1,3]dioxol-5-yl)(morpholino)methanone

생성물 1

HCID 21865380(3,4-Dihydroxyphenyl)(morpholino)methanone수율 95%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
0 °C

실험 절차

To a cooled (0° C.) solution of (2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanone (270 mg, 0.7 mmol) in trifluoroacetic acid (4 mL) was added triethylsilane (160 mg, 1.38 mmol, 1.96 eq.). The reaction mixture was stirred 20 min at 0° C. The cooling bath was removed and the reaction mixture was stirred for 4 h at R.T. The reaction mixture was evaporated. Purification by flash chromatography afforded the title compound (147 mg, 95%) as a white solid.

후처리

  1. customThe cooling bath was removed
  2. stirringthe reaction mixture was stirred for 4 h at R.T
  3. customThe reaction mixture was evaporated
  4. customPurification by flash chromatography

출처 및 근거

ORD 기록
ord-06046566397044619b8759febee9891c
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576088B2

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