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Methanol → Isoquinoline-6-carboxaldehyde

HRID 598823
ノート
印刷プレビュー

反応式

HRID 598823 の反応式
[CH:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[N:8][CH:7]=[CH:6]2)=C.C[OH:14]>C(Cl)Cl>[CH:9]1[C:10]2[C:5](=[CH:4][C:3]([CH:1]=[O:14])=[CH:12][CH:11]=2)[CH:6]=[CH:7][N:8]=1
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

4

反応物 2

HCID 887MethanolHCID 579507066-Vinylisoquinoline

生成物 1

HCID 15290359Isoquinoline-6-carboxaldehyde収率 94%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

To a 150 mL round-bottomed flask was added 6-vinylisoquinoline (2.47 g, 16 mmol) and MeOH (35 mL)/DCM (35 mL). The resulting solution was cooled to −78° C. The reaction was ozonized until a blue color persisted, then nitrogen gas was bubbled through the solution for 15 minutes to purge the ozone. The reaction was then treated with solid sodium bicarbarbonate. (1.5 g) and dimethyl sulfide (3.2 mL, 0.2 mL/mmol of SM) and the mixture was warmed to room temperature and stirred overnight. The reaction mixture was diluted with water (100 mL) and extracted with DCM (3×75 mL). The combined organic layers were dried over Na2SO4, filtered, and the residue product isoquinoline-6-carbaldehyde (2.35 g, 94% yield) was used without further manipulation. LCMS (API-ES) m/z (%): 158.1 (100%, M++H).

後処理

  1. customnitrogen gas was bubbled through the solution for 15 minutes
  2. customto purge the ozone
  3. additionThe reaction was then treated with solid sodium bicarbarbonate
  4. temperature(1.5 g) and dimethyl sulfide (3.2 mL, 0.2 mL/mmol of SM) and the mixture was warmed to room temperature
  5. additionThe reaction mixture was diluted with water (100 mL)
  6. extractionextracted with DCM (3×75 mL)
  7. dry with materialThe combined organic layers were dried over Na2SO4
  8. filtrationfiltered

出典と根拠

ORDレコード
ord-fd7334d1f8dd4f9791049e5168ac5b66
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07897619B2

反応ノート

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