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

HRID 886020
ノート
印刷プレビュー

反応式

HRID 886020 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6228DimethylformamideHCID 25517Ammonium ChlorideHCID 587641932-chloro-5-(MethoxyMethoxy)pyridineHCID 178418306HCID 178418306、化合物

生成物 1

HCID 582044792-Chloro-5-(methoxymethoxy)isonicotinaldehyde

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8003
Pentane
溶媒

反応条件

温度
-76 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e7ee7a9678284140a54cf3ed19c320f3
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08242104B2

反応ノート

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