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Sodium borohydride → [3,3'-Bipyridin]-5-ylmethanol

HRID 353782
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HRID 353782 반응식
C([O:3][C:4]([C:6]1[CH:7]=[C:8]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[CH:9]=[N:10][CH:11]=1)=O)C.[BH4-].[Na+]>C(O)C>[N:10]1[CH:11]=[C:6]([CH2:4][OH:3])[CH:7]=[C:8]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[CH:9]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 11535941HCID 11535941, 화합물

생성물 1

HCID 11528472[3,3'-Bipyridin]-5-ylmethanol수율 34%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
50 °C

실험 절차

To a solution of [3,3′]bipyridinyl-5-carboxylic acid ethyl ester (1 eq) in ethanol was added sodium borohydride (2 eq) at room temperature. The reaction mixture was heated in a 50° C. oil bath for 60 minutes and then quenched by addition of H2O. Once the reaction solvent was removed in vacuo, a solution of the residue in dichloromethane was washed with NaCl(sat), dried over sodium sulfate, filtered and concentrated. The crude solid was purified by flash chromatography using a solvent gradient of 95% DCM, 5% MeOH and 0.1% TEA to yield [3,3′]bipyridinyl-5-yl-methanol (34%). MH+(187).

후처리

  1. customquenched by addition of H2O
  2. customOnce the reaction solvent was removed in vacuo
  3. washa solution of the residue in dichloromethane was washed with NaCl(sat)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude solid was purified by flash chromatography

출처 및 근거

ORD 기록
ord-c0ba1c77dc444c77aca02363892dad35
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06756359B2

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