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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Bromopyridine-4-carboxaldehyde → (3-Bromopyridin-4-yl)methanol

HRID 593584
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HRID 593584 반응식
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH:8]=[O:9].[BH4-].[Na+]>CO>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][OH:9]
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참가 물질

4

반응물 2

HCID 27629973-Bromopyridine-4-carboxaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 46840038(3-Bromopyridin-4-yl)methanol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3-bromo-pyridine-4-carbaldehyde (0.500 g, 2.68 mmol) in MeOH (5 mL) at 0° C. is added sodium borohydride (0.122 g, 3.22 mmol). The mixture is stirred at room temperature for 1 h followed by removal of the solvent in vacuo. The residue is redissolved in DCM and washed with water twice. The organic layer is dried over sodium sulfate and concentrated in vacuo to afford (3-bromo-pyridin-4-yl)-methanol as a yellow oil. MS (ESI) m/z 189.9 (M+H)+

후처리

  1. customfollowed by removal of the solvent in vacuo
  2. dissolutionThe residue is redissolved in DCM
  3. washwashed with water twice
  4. dry with materialThe organic layer is dried over sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-196e5af2399b48d5b099b41a5f155237
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242963B2

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