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Aluminium lithium hydride → 2-(Quinolin-5-yl)propan-1-ol

HRID 1814306
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HRID 1814306 반응식
[N:1]1[C:10]2[C:5](=[C:6]([CH:11]([CH3:16])[C:12](OC)=[O:13])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[N:1]1[C:10]2[C:5](=[C:6]([CH:11]([CH3:16])[CH2:12][OH:13])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 22504014Methyl 2-(quinolin-5-yl)propanoate

생성물 1

HCID 225040802-(Quinolin-5-yl)propan-1-ol수율 74%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

Methyl 2-(5-quinolyl)propanoate (100 mg, 0.47 mmol) was dissolved in dry THF(10 mL) and cooled to −78° C. on a dry ice/acetone bath. Lithium aluminum hydride (1M in ether, 0.93 mL, 0.93 mmol) was added dropwise. The mixture stirred for 10 minutes while warming to 0° C. The reaction was quenched with KHSO4(1M aq., 1 mL). The mixture was made basic with NaOH(1M aq) and extracted into ethyl acetate. The organics were washed with brine, dried over MgSO4 and then removed under reduced pressure to give 2-(5-quinolyl)-1-propanol (65 mg, 74%). HPLC (10% to 90% acetonitrile in 0.1N aqueous ammonium acetate over 10 min at 2 mL/min using a waters Symmetry C18, 150×4.6 mm column) 2.96 min.

후처리

  1. temperaturewhile warming to 0° C
  2. customThe reaction was quenched with KHSO4(1M aq., 1 mL)
  3. extractionextracted into ethyl acetate
  4. washThe organics were washed with brine
  5. dry with materialdried over MgSO4
  6. customremoved under reduced pressure

출처 및 근거

ORD 기록
ord-616261477f8e49c4a8a897d8a58bc90f
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06875765B2

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