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Nitric Acid → HCID 59547210、化合物

HRID 2408955
ノート
印刷プレビュー

反応式

HRID 2408955 の反応式
[CH3:1][C:2]1[Se:6][C:5]([C:7]([O:9][CH3:10])=[O:8])=[CH:4][CH:3]=1.[N+:11]([O-])([OH:13])=[O:12]>C(OC(=O)C)(=O)C>[CH3:1][C:2]1[Se:6][C:5]([C:7]([O:9][CH3:10])=[O:8])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12]
参加物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 944Nitric AcidHCID 13637637HCID 13637637、化合物

生成物 1

HCID 59547210HCID 59547210、化合物収率 35%

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒2 回

実験手順

To an ice cold (0-10° C.) solution of methyl 5-methylselenophene-2-carboxylate (5.4 g, 26.6 mmol) in acetic anhydride (15 mL) was added an ice cold mixture of nitric acid (5.5 mL, 61.1 mmol, 70%) and acetic anhydride (10 mL) for 10 min. The reaction mixture was slowly allowed to rt for 1 h and stirred at room temperature (rt) for 16 h. The mixture was poured into ice cold water and stirred for 10 min. The solution was extracted with chloroform (3×100 mL) and the combined organic layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (90:10) as eluents to give the product as an pale yellow color solid (2.3 g, 35%), mp 90-92° C. 1H NMR (400 MHz, CDCl3): δ 8.54 (1H, s), 3.90 (3H, s), 2.90 (3H, s).

後処理

  1. additionThe mixture was poured into ice cold water
  2. stirringstirred for 10 min
  3. extractionThe solution was extracted with chloroform (3×100 mL)
  4. washthe combined organic layer was washed with water, brine
  5. dry with materialdried over sodium sulfate
  6. filtrationThe solution was filtered
  7. customevaporated the solvent
  8. customThe residue was chromatographed over silica gel column

出典と根拠

ORDレコード
ord-503d9f64a8cc4194be0c5913cc23683d
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815879B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート