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Acetic Acid → HCID 53730400、化合物

HRID 650061
ノート
印刷プレビュー

反応式

HRID 650061 の反応式
[C:1]([O:8][CH2:9][CH3:10])(=[O:7])[C:2]([O:4]CC)=O.[CH3:11][C:12]1[C:17]([N+:18]([O-:20])=[O:19])=[C:16]([N:21]([CH3:31])[CH2:22][CH2:23][O:24][CH:25]2[CH2:30][CH2:29][CH2:28][CH2:27][O:26]2)[CH:15]=[CH:14][C:13]=1[C:32]([F:35])([F:34])[F:33].[O-]CC.[K+].C(O)(=O)C>O1CCCC1.O>[CH3:31][N:21]([C:16]1[C:17]([N+:18]([O-:20])=[O:19])=[C:12]([CH2:11][C:2](=[O:4])[C:1]([O:8][CH2:9][CH3:10])=[O:7])[C:13]([C:32]([F:34])([F:35])[F:33])=[CH:14][CH:15]=1)[CH2:22][CH2:23][O:24][CH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][O:26]1
参加物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 176Acetic AcidHCID 7268Diethyl OxalateHCID 21714329HCID 21714329、化合物HCID 23670592Potassium ethoxide

生成物 1

HCID 53730400HCID 53730400、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

Diethyl oxalate (1.94 g, 13.2 mmol) and then a solution of 2-methyl-4-[N-methyl-N-[2-(2-tetrahydro-2H-pyranyl)oxyethyl]amino]-3-nitrobenzotrifluoride (2.40 g, 6.62 mmol) in tetrahydrofuran (40 ml) were added dropwise to a mixture of potassium ethoxide (1.11 g, 13.2 mmol) and tetrahydrofuran (60 ml) at room temperature. The reaction mixture was stirred at room temperature for 6 hours and then cooled to 3° C., and acetic acid (1.59 g, 26.5 mmol) was added dropwise. The reaction mixture thus obtained was poured into cold water and extracted twice with ethyl acetate. The extract solution was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/9) to obtain an oil of ethyl [3-[N-methyl-N-[2-(2-tetrahydro-2H-pyranyl)oxyethyl]amino]-2-nitro-6-trifluoromethylphenyl]pyruvate.

後処理

  1. temperaturecooled to 3° C.
  2. customThe reaction mixture thus obtained
  3. extractionextracted twice with ethyl acetate
  4. washThe extract solution was washed with a 5% aqueous sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure
  7. customthe resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/9)

出典と根拠

ORDレコード
ord-b53fc2921f9142578af37e1dc3f7059b
出典データセット
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06271251B1

反応ノート

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