Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate

HRID 34470

反応式

HRID 34470 の反応式
[C:1]([C:3](=[CH:9][C:10]1[C:15]2[CH:16]=[CH:17][CH2:18][O:19][C:14]=2[C:13]([O:20][CH3:21])=[C:12]([O:22][CH3:23])[CH:11]=1)[C:4]([O:6][CH2:7][CH3:8])=[O:5])#[N:2].C(O)(=O)C.CC1C(Br)=C(O)C(Br)=CC=1C1(C2C=C(Br)C(O)=C(Br)C=2C)OS(=O)(=O)C2C=CC=CC1=2.C([BH3-])#N.[Na+]>C(O)C>[C:1]([CH:3]([CH2:9][C:10]1[C:15]2[CH:16]=[CH:17][CH2:18][O:19][C:14]=2[C:13]([O:20][CH3:21])=[C:12]([O:22][CH3:23])[CH:11]=1)[C:4]([O:6][CH2:7][CH3:8])=[O:5])#[N:2]

参加物

6

実験手順

A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acetic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.

後処理

  1. temperatureHeating
  2. customthe ethanol removed under reduced pressure
  3. extractionsuccessively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL)
  4. dry with materialdried over magnesium sulfate
  5. customThe volatiles were removed under reduced pressure
  6. customto leave an amber oil, 18.22 g (91.4%) which
  7. customwas used without further purification

出典と根拠

ORDレコード
ord-62b182c93158406b8248468834a06f6a
出典データセット
uspto-grants-1988_08
特許番号
US04761475

関連ノート

読み込み中…