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Dimethylformamide → 2-Chloro-5-(methoxymethoxy)isonicotinaldehyde

HRID 2044237
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인쇄 미리보기

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HRID 2044237 반응식
C([Li])(C)(C)C.[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][O:15][CH3:16])=[CH:9][N:8]=1.CN(C)[CH:19]=[O:20].[NH4+].[Cl-]>CCCCC.C(OCC)C>[Cl:6][C:7]1[CH:12]=[C:11]([C:10]([O:13][CH2:14][O:15][CH3:16])=[CH:9][N:8]=1)[CH:19]=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 25517Ammonium ChlorideHCID 587641932-chloro-5-(MethoxyMethoxy)pyridineHCID 178418306HCID 178418306, 화합물

생성물 1

HCID 582044792-Chloro-5-(methoxymethoxy)isonicotinaldehyde

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8003
Pentane
용매

반응 조건

온도
-76 °C

실험 절차

tert-Butyllithium in pentane (1.7 M, 19.0 mL) was added dropwise to a solution of 2-chloro-5-(methoxymethoxy)pyridine (4.880 g, 28.11 mmol) in 100 ml of ethyl ether at −76° C. Some precipitate appeared. The mixture was kept at −76° C. for 20 min then N,N-dimethylformamide (2.938 mL, 37.95 mmol) was added dropwise. The mixture was stirred for 10 min at −76° C. and then allowed to warm to at 0° C. for 1 h period. 10% aq NH4Cl was added and the mixture was extracted with ethyl acetate. The organic solution was washed with water, brine and dried over Na2SO4. After concentration in vacuum the yield of the crude 2-chloro-5-(methoxymethoxy)isonicotinaldehyde 5.49 g. MS: 202.0, 172.0. Without further purification was used in the next step.

후처리

  1. temperatureto warm to at 0° C. for 1 h period
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic solution was washed with water, brine
  4. dry with materialdried over Na2SO4
  5. concentrationAfter concentration in vacuum the yield of the crude 2-chloro-5-(methoxymethoxy)isonicotinaldehyde 5.49 g
  6. customWithout further purification

출처 및 근거

ORD 기록
ord-4048d89f5b23438c91956c3ed7af1456
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586574B2

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