Diethyl squarate → 4-(2-Ethoxy-3,4-dioxo-cyclobut-1-enylamino)-3-ethylbenzonitrile

HRID 1733900

反応式

HRID 1733900 の反応式
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[CH2:10][CH3:11].[CH2:12]([O:14][C:15]1[C:16](=O)[C:17](=[O:22])[C:18]=1[O:19]CC)[CH3:13]>C(#N)C.C(OCC)(=O)C>[O:19]=[C:18]1[C:17](=[O:22])[C:16]([NH:1][C:2]2[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=2[CH2:10][CH3:11])=[C:15]1[O:14][CH2:12][CH3:13]

参加物

5

反応物 2

HCID 123228Diethyl squarate2 回HCID 27353304-Amino-3-ethylbenzonitrile

生成物 1

HCID 199729184-(2-Ethoxy-3,4-dioxo-cyclobut-1-enylamino)-3-ethylbenzonitrile収率 24%

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

4-Amino-3-ethylbenzonitrile (2.00 g, 13.7 mmol) was added to a solution of 3,4-diethoxy-3-cyclobutene-1,2-dione (2.30 g, 13.5 mmol) in acetonitrile (5 mL). After refluxing the mixture for 24 h a second portion of 3,4-diethoxy-3-cyclobutene-1,2-dione (1.15 g, 6.76 mmol) was added and heating was continued for an additional 24 h. The reaction mixture was diluted with ethyl acetate (45 mL), stirred vigorously and filtered free of undissolved solid. The filtrate was concentrated and the resulting residue was purified by chromatographed (CH3OH/CH2Cl2) and trituration with ether to afford 0.86 g (24%) of product as a light yellow solid: 1H NMR (DMSO-d6): δ 10.57 (s, 1H), 7.77-7.66 (m, 2H), 7.31 (d, 1H), 4.71 (q, 2H), 2.73 (q, 2H), 1.37 (t, 3H), 1.13 (t, 3H).

後処理

  1. additionwas added
  2. temperatureheating
  3. filtrationfiltered free of undissolved solid
  4. concentrationThe filtrate was concentrated
  5. customthe resulting residue was purified
  6. customby chromatographed (CH3OH/CH2Cl2) and trituration with ether

出典と根拠

ORDレコード
ord-cc97b40a15064c2d81a778b15be983aa
出典データセット
uspto-grants-1996_07
特許番号
US05532245

関連ノート

読み込み中…