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Acetone → 2-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-ol

HRID 1455648
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HRID 1455648 반응식
[S:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Li]CCCC.[CH3:11][C:12]([CH3:14])=[O:13].[CH2:15]([Sn:19](Cl)([CH2:24][CH2:25][CH2:26][CH3:27])[CH2:20][CH2:21][CH2:22][CH3:23])[CH2:16][CH2:17][CH3:18].[NH4+].[Cl-]>C1COCC1.CCOCC>[CH2:24]([Sn:19]([CH2:15][CH2:16][CH2:17][CH3:18])([CH2:20][CH2:21][CH2:22][CH3:23])[C:5]1[S:1][C:2]([C:12]([OH:13])([CH3:14])[CH3:11])=[N:3][CH:4]=1)[CH2:25][CH2:26][CH3:27]
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참가 물질

8

반응물 5

HCID 180AcetoneHCID 9256ThiazoleHCID 15096Tributyltin ChlorideHCID 25517Ammonium ChlorideHCID 178418339Butyllithium2회

생성물 1

HCID 468400252-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-ol

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a solution of thiazole (1.0 eq) in THF (0.2M) at −78° C. was added nBuLi (1.6M, 1.1 eq). After 1 h at −78° C., acetone (1.0 eq) was added and the mixture stirred 30 min at −78° C., 5 min −50° C. then cooled back to −78° C. to add a second equivalent of nBuLi (1.6M, 1.1 eq). After 1.5 h at −78° C., tri-n-butyltin chloride (1.2 eq) was added and the mixture stirred 12 h at −78° C. The reaction mixture was diluted with Et2O and a solution of NH4Cl. The organic extracts were washed with water, brine, dried over MgSO4, filtered and concentrated. Flash chromatography (Hexane:EtOAc, 90:10) afforded the title compound.

후처리

  1. temperature5 min −50° C. then cooled back to −78° C.
  2. waitAfter 1.5 h at −78° C.
  3. stirringthe mixture stirred 12 h at −78° C
  4. washThe organic extracts were washed with water, brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f6ba3af8f1cf4d8f9ace31be503e443d
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482456B2

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