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Water → 2,5-Dichloro-6-methoxy-4-methylnicotinonitrile

HRID 656633
ノート
印刷プレビュー

反応式

HRID 656633 の反応式
[Cl:1][C:2]1[N:9]=[C:8](Cl)[C:7]([Cl:11])=[C:6]([CH3:12])[C:3]=1[C:4]#[N:5].[CH3:13][O-:14].[Na+].O>CO>[Cl:1][C:2]1[N:9]=[C:8]([O:14][CH3:13])[C:7]([Cl:11])=[C:6]([CH3:12])[C:3]=1[C:4]#[N:5]
参加物反応条件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 962WaterHCID 10942334Sodium MethoxideHCID 336978792,5,6-Trichloro-4-methylnicotinonitrile

生成物 1

HCID 534158922,5-Dichloro-6-methoxy-4-methylnicotinonitrile収率 93.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

To a slurry of 2,5,6-trichloro-4-methyl-nicotinonitrile (11.0 g, 49.67 mmol, Tetrahedron, 1977, 33, 113-117) in MeOH (125 ml) is added sodium methoxide solution (25% wt. in MeOH)(11.92 ml, 52.15 mmol). The reaction mixture is stirred at 0° C. for 30 minutes, then room temperature for 1 hour. The reaction is quenched by the addition of water (300 ml) and a thick, white precipitate is formed. An additional 200 ml of water is added and the mixture is stirred at 0° C. for 10 minutes. The precipitate is collected by filtration and dried (vacuum oven for 16 hours at 60° C.) to give the title compound as an off-white solid (10.05 g, 93%). Mass (m/z): 217.0 (M++1).

後処理

  1. waitroom temperature for 1 hour
  2. customThe reaction is quenched by the addition of water (300 ml)
  3. customa thick, white precipitate is formed
  4. stirringthe mixture is stirred at 0° C. for 10 minutes
  5. filtrationThe precipitate is collected by filtration
  6. customdried (vacuum oven for 16 hours at 60° C.)

出典と根拠

ORDレコード
ord-d6499da99bf3479daa68671392cd9511
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071776B2

反応ノート

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