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Tetrabutylammonium Fluoride → HCID 18950583, 화합물

HRID 1492577
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HRID 1492577 반응식
[Si]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][N:16]2[C:20]3=[N:21][C:22]([CH3:26])=[CH:23][C:24]([CH3:25])=[C:19]3[N:18]=[C:17]2[CH2:27][CH3:28])=[CH:11][C:10]=1[Cl:29])(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[Cl:29][C:10]1[CH:11]=[C:12]([CH2:15][N:16]2[C:20]3=[N:21][C:22]([CH3:26])=[CH:23][C:24]([CH3:25])=[C:19]3[N:18]=[C:17]2[CH2:27][CH3:28])[CH:13]=[CH:14][C:9]=1[OH:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 19385593HCID 19385593, 화합물

생성물 1

HCID 18950583HCID 18950583, 화합물수율 90.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 0.294 g (0.661 mmol) of the product of Step D dissolved in 4 mL of THF was added 0.69 mL (0.69 mmol) of a 1.0M solution of tetra-n-butylammonium fluoride in THF, and the reaction mixture was stirred 2 hours at room temperature. The reaction was then concentrated in vacuo and purified by filtration through a silica gel pad eluted with chloroform. Evaporation of the filtrate and drying in vacuo afforded 0.188 g (87%) of the title compound.

후처리

  1. concentrationThe reaction was then concentrated in vacuo
  2. filtrationpurified by filtration through a silica gel pad
  3. washeluted with chloroform
  4. customEvaporation of the filtrate
  5. customdrying in vacuo

출처 및 근거

ORD 기록
ord-62a579d115384adb832c409c4998fedb
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374638

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