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Sodium hydride → HCID 131734716、化合物

HRID 1774003
ノート
印刷プレビュー

反応式

HRID 1774003 の反応式
[I-].[CH3:2][S+](C)(C)=O.[H-].[Na+].[CH3:9][O:10][N:11]([CH3:22])[C:12](=[O:21])/[CH:13]=[CH:14]/[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=1>CS(C)=O.[NH4+].[Cl-]>[CH3:9][O:10][N:11]([CH3:22])[C:12]([C@@H:13]1[CH2:2][C@H:14]1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=1)=[O:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 24758Sodium hydrideHCID 74498Sulfoxonium, trimethyl-, iodide (1:1)HCID 89648964HCID 89648964、化合物

生成物 1

HCID 131734716HCID 131734716、化合物

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒2 回HCID 25517Ammonium Chloride溶媒

実験手順

To a solution under N2 of trimethylsulfoxonium iodide (3.89 g, 17.7 mmol, 2 eq.) in DMSO (10 mL) cooled at r.t. with a water bath, sodium hydride 60% dispersion in mineral oil (707 mg, 17.7 mmol, 2 eq.) was added portionwise over 10 min. The resulting mixture was stirred at r.t. for 1 hour. A solution of (E)-N-methoxy-N-methyl-3-(pyridin-2-yl)acrylamide (1.70 g, 8.8 mmol, 1 eq.) in DMSO (5 mL) was added and the reaction mixture was stirred at r.t. for 18 hours. The reaction mixture was poured in sat. aq. NH4Cl soln. (50 mL) and extracted with DCM (3×50 mL). The comb. org. phases were washed with sat. aq. NaCl soln. (1×50 mL), dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by flashmaster (column: 100 g, flow: 45 mL/min, 30 fractions of 45 mL, Heptane+20% AcOEt to Heptane+80% AcOEt) to yield (±)-(trans)-2-pyridin-2-yl-cyclopropanecarboxylic acid methoxy-methyl-amide as an yellow oil.

後処理

  1. stirringthe reaction mixture was stirred at r.t. for 18 hours
  2. extraction(50 mL) and extracted with DCM (3×50 mL)
  3. washphases were washed with sat. aq. NaCl soln
  4. dry with material(1×50 mL), dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flashmaster (column: 100 g, flow: 45 mL/min, 30 fractions of 45 mL, Heptane+20% AcOEt to Heptane+80% AcOEt)

出典と根拠

ORDレコード
ord-adc58ceab3e44661a730c53bcb5e2824
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09255090B2

反応ノート

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