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Formic Acid → 4-(8-Methyl-8-azabicyclo[3.2.1]oct-3-yloxy)benzaldehyde

HRID 1949991
ノート
印刷プレビュー

反応式

HRID 1949991 の反応式
[CH3:1][N:2]1[CH:7]2[CH2:8][CH2:9][CH:3]1[CH2:4][CH:5]([O:10][C:11]1[CH:18]=[CH:17][C:14]([C:15]#N)=[CH:13][CH:12]=1)[CH2:6]2.C(O)=[O:20]>[Ni]>[CH3:1][N:2]1[CH:7]2[CH2:8][CH2:9][CH:3]1[CH2:4][CH:5]([O:10][C:11]1[CH:18]=[CH:17][C:14]([CH:15]=[O:20])=[CH:13][CH:12]=1)[CH2:6]2
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 284Formic AcidHCID 113569274-(8-Methyl-8-azabicyclo[3.2.1]oct-3-yloxy)benzonitrile

生成物 1

HCID 579340574-(8-Methyl-8-azabicyclo[3.2.1]oct-3-yloxy)benzaldehyde

試薬・触媒・溶媒 1

HCID 935Nickel触媒

反応条件

温度
100 °C

実験手順

The title compound was synthesized by referring to Chem. Pharm. Bull., 1991, 39, 1440. To a solution of 4-(8-methyl-8-azabicyclo[3.2.1]oct-3-yloxy)benzonitrile (300 mg) in formic acid (5 ml) was added Raney nickel (50% suspension in water) (1 ml), and the solution was stirred for 2 hours at 100° C. After filtration through celite pad and several wash with tetrahydrofuran and methanol, the solvent was evaporated in vacuo, and the resulting residue was neutralized by adding a saturated aqueous solution of sodium bicarbonate. After extraction with chloroform and washing with brine, the solution was dried over anhydrous magnesium sulfate, then the solvent was evaporated in vacuo to provide the title compound (266 mg).

後処理

  1. customThe title compound was synthesized
  2. filtrationAfter filtration through celite pad
  3. washseveral wash with tetrahydrofuran and methanol
  4. customthe solvent was evaporated in vacuo
  5. additionby adding a saturated aqueous solution of sodium bicarbonate
  6. extractionAfter extraction with chloroform
  7. washwashing with brine
  8. dry with materialthe solution was dried over anhydrous magnesium sulfate
  9. customthe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-39780429502f4948bd70166bfcf2e30a
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399520B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート