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Diisobutylaluminumhydride → HCID 11264243, 화합물

HRID 1006139
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HRID 1006139 반응식
[H-].C([Al+]CC(C)C)C(C)C.C([O:13][C:14]([C:16]1[CH:25]=[C:24]2[C:19]([C:20]([Cl:27])=[CH:21][C:22]([CH3:26])=[N:23]2)=[CH:18][CH:17]=1)=O)C>O1CCCC1>[Cl:27][C:20]1[C:19]2[C:24](=[CH:25][C:16]([CH2:14][OH:13])=[CH:17][CH:18]=2)[N:23]=[C:22]([CH3:26])[CH:21]=1
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참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 24278901HCID 24278901, 화합물

생성물 1

HCID 11264243HCID 11264243, 화합물수율 71.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

Diisobutylaluminum hydride (1 M solution in tetrahydrofuran, 80 mL, 80 mmol) was added dropwise at 0° C. to a solution of 4-chloro-2-methyl-quinoline-7-carboxylic acid ethyl ester (4.42 g, 17.7 mmol) in tetrahydrofuran (90 mL), then after stirring 1 h at 0° C. the reaction was quenched by careful addition of methanol (4.5 mL) and 1 M aq. potassium sodium tartrate solution (135 mL). The two-phase mixture was stirred 30 min, then extracted twice with ethyl acetate. The organic phases were washed with brine, dried (MgSO4) and evaporated. Chromatography (SiO2, hexane/ethyl acetate 1:1 afforded the title compound (2.62 g, 71%). Off-white solid, EI-MS: m/e==207.2 (M30 ).

후처리

  1. customwas quenched by careful addition of methanol (4.5 mL) and 1 M aq. potassium sodium tartrate solution (135 mL)
  2. stirringThe two-phase mixture was stirred 30 min
  3. extractionextracted twice with ethyl acetate
  4. washThe organic phases were washed with brine
  5. dry with materialdried (MgSO4)
  6. customevaporated

출처 및 근거

ORD 기록
ord-df751875a3914ea8b67ecae796b49a3d
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06787558B2

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