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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetone → 5-Chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde

HRID 420728
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HRID 420728 반응식
C(O)(=O)C(O)=O.[Cl:7][C:8]1[C:9]([CH2:19][OH:20])=[N:10][CH:11]=[C:12]([CH:14]2OCC[O:15]2)[CH:13]=1.CC(C)=O.[OH-].[Na+]>O>[Cl:7][C:8]1[CH:13]=[C:12]([CH:14]=[O:15])[CH:11]=[N:10][C:9]=1[CH2:19][OH:20]
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참가 물질

6

반응물 4

HCID 180AcetoneHCID 971Oxalic AcidHCID 14798Sodium HydroxideHCID 66658029HCID 66658029, 화합물

생성물 1

HCID 580017855-Chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde수율 10%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Oxalic acid (415 mg, 3.29 mmol) was added to a mixture of [3-chloro-5-(1,3-dioxolan-2-yl)-2-pyridinyl]methanol (142 mg, 0.659 mmol), acetone (7.5 ml), and water (7.5 ml) at room temperature and heated under reflux. After 2.5 h, HPLC showed full conversion. Cooled to rt, basified with 1M NaOH, extracted with TBME, dried (MgSO4), filtered and concentrated to give 139 mg of crude material. Purification by flash chromatography using Flashmaster II, a 5 g silica gel cartridge, and mixtures of DCM and MeOH as eluent afforded impure product. Repurification by manual flash chromatography using a 1 g silica gel cartridge, and mixtures of hexane and EtOAc as eluent afforded 5-chloro-6-(hydroxymethyl)-3-pyridinecarbaldehyde (11.3 mg, 10%) as a white solid.

후처리

  1. temperatureheated
  2. temperatureunder reflux
  3. extractionextracted with TBME
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give 139 mg of crude material
  8. customPurification by flash chromatography
  9. customa 5 g silica gel cartridge, and mixtures of DCM and MeOH as eluent afforded impure product
  10. customRepurification by manual flash chromatography

출처 및 근거

ORD 기록
ord-1aa3307aa8d3482fb0ce7a6283c7b964
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097628B2

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