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Hydrochloric Acid → HCID 59547213、化合物

HRID 2408956
ノート
印刷プレビュー

反応式

HRID 2408956 の反応式
[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-])=O.Cl.[Cl-].[NH4+]>O.CO.[Fe]>[NH2:11][C:3]1[CH:4]=[C:5]([C:7]([O:9][CH3:10])=[O:8])[Se:6][C:2]=1[CH3:1]
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 3

HCID 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 59547210HCID 59547210、化合物

生成物 1

HCID 59547213HCID 59547213、化合物収率 79%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 887Methanol溶媒
HCID 962
Water
溶媒

実験手順

To a solution of methyl 5-methyl-4-nitroselenophene-2-carboxylate (2.3 g, 9.28 mmol) in a mixture of water (5 mL) and methanol (40 mL) was added conc. hydrochloric acid (1.0 mL). To the above solution was added iron powder (2.6 g, 46.4 mmol) followed by ammonium chloride (2.5 g, 46.4 mmol) at rt. The reaction mixture was refluxed for 1 h and was then allowed to cool to rt. The solution was filtered and basified with saturated sodium bicarbonate solution. The solution was extracted with ethyl acetate (4×100 mL) and the combined organic layer was dried over sodium sulfate and filtered. Solvent was evaporated and the residue was chromatographed over silica gel column using hexane-ethyl acetate (80:20) as eluent to give methyl 4-amino-5-methylselenophene-2-carboxylate (1.6 g, 79%), mp 66-68° C. 1H NMR (400 MHz, DMSO-d6): δ 7.57 (1H, s), 4.72 (2H, br s), 3.73 (3H, s), 2.24 (3H, s).

後処理

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. filtrationThe solution was filtered
  3. extractionThe solution was extracted with ethyl acetate (4×100 mL)
  4. dry with materialthe combined organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. customSolvent was evaporated
  7. customthe residue was chromatographed over silica gel column

出典と根拠

ORDレコード
ord-4e0fe5d4c4844ab3a2a94f1e61379192
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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