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Ethanol → HCID 86742227、化合物

HRID 580216
ノート
印刷プレビュー

反応式

HRID 580216 の反応式
[Cl-].[NH4+:2].[CH3:3][O:4][N:5]=[C:6]([C:9]#[N:10])[C:7]#[N:8].[CH2:11]([OH:13])[CH3:12]>N>[C:11]([O-:4])(=[O:13])[CH3:12].[C:7]([C:6](=[N:5][O:4][CH3:3])[C:9]([NH2:2])=[NH2+:10])#[N:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 702Ethanol2 回HCID 25517Ammonium ChlorideHCID 12474891Methoxyiminomalononitrile

生成物 1

HCID 86742227HCID 86742227、化合物

試薬・触媒・溶媒 1

HCID 222Ammonia溶媒

実験手順

To a solution of ammonium chloride (28.4 g 0.53 mole) in 28% aqueous ammonia (355 ml) and ethanol (180 ml) was added dropwise a solution of 2-methoxyiminopropanedinitrile (58.0 g, 0.53 mole) in ethanol (120 ml) at -15° to -10° C. over a period of 30 minutes, with stirring. The mixture was stirred at -10° C. overnight and then at ambient temperature (20°-25° C.) for one day. The reaction mixture was partitioned between water (350 ml) and CH2Cl2 (350 ml), and the aqueous phase was saturated with sodium chloride, and extracted again with CH2Cl2 (300 ml). The organic extracts were combined, dried over MgSO4 and evaporated in vacuo. A solution of the residue in ethyl acetate (1.6 L) was adjusted to pH 3-4 with acetic acid to precipitate the title compound as crystals, which were collected by filtration and washed with ethyl acetate. Yield 67.6 g (69%). M.p. 152°-4° C. (dec.). [Lit., m.p. 150°-155° C. (dec.)].

後処理

  1. stirringThe mixture was stirred at -10° C. overnight
  2. customThe reaction mixture was partitioned between water (350 ml) and CH2Cl2 (350 ml)
  3. extractionextracted again with CH2Cl2 (300 ml)
  4. dry with materialdried over MgSO4
  5. customevaporated in vacuo
  6. customto precipitate the title compound as crystals, which
  7. filtrationwere collected by filtration
  8. washwashed with ethyl acetate

出典と根拠

ORDレコード
ord-eb7d335c3c3b495f91b7e397a9b2739c
出典データセット
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04751295

反応ノート

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