Cyanogen Bromide → 2,2-Dimethoxy-1-methylpropylcyanamide

HRID 615262ノート

反応式

HRID 615262 の反応式
[N:1]#[C:2]Br.[CH3:4][O:5][C:6]([O:11][CH3:12])([CH3:10])[CH:7]([NH2:9])[CH3:8]>O.CO>[CH3:4][O:5][C:6]([O:11][CH3:12])([CH3:10])[CH:7]([NH:9][C:2]#[N:1])[CH3:8]

参加物

5

反応物 2

HCID 10476Cyanogen BromideHCID 158518261-Methyl-2,2-dimethoxypropylamine

生成物 1

HCID 201644792,2-Dimethoxy-1-methylpropylcyanamide

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒2 回

実験手順

Cyanogen bromide (424 mg., 4 m moles) was added to a solution of 2,2-dimethoxy-1-methylpropylamine (266 mg., 2 m moles) and KHCO3 (400 mg., 4 m moles) in a mixture of water (2 ml.) and methanol (4 ml.). After 15 minutes the mixture was poured into water (150 ml.) and the mixture extracted with CH2Cl2. The extract was washed with water and brine, dried (MgSO4) and evaporated to dryness to give 2,2-dimethoxy-1-methylpropylcyanamide as a pale yellow oil (280 mg., 88%) having the following n.m.r. spectrum in CDCl3 : 1.15 (s, 3H), 1.18 (d, 3H); 3.15 (s, 6H); 3.0-3.6 (m, 1H); 4.0 (m, 1H).

後処理

  1. extractionthe mixture extracted with CH2Cl2
  2. washThe extract was washed with water and brine
  3. dry with materialdried (MgSO4)
  4. customevaporated to dryness

出典と根拠

ORDレコード
ord-b33e2376a4334f72a40abad4790fb097
出典データセット
uspto-grants-1985_02
特許番号
US04497949

反応ノート

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