Acetic Acid → 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-methylamino-4-trifluoromethylsulfonylpyrazole

HRID 987073ノート

反応式

HRID 987073 の反応式
[C:1]([C:3]1[C:7]([S:8]([C:10]([F:13])([F:12])[F:11])=[O:9])=[C:6]([N:14]=[CH:15]OCC)[N:5]([C:19]2[C:24]([Cl:25])=[CH:23][C:22]([C:26]([F:29])([F:28])[F:27])=[CH:21][C:20]=2[Cl:30])[N:4]=1)#[N:2].[BH4-].[Na+].C(O)(=[O:35])C>C(O)C>[C:1]([C:3]1[C:7]([S:8]([C:10]([F:12])([F:13])[F:11])(=[O:35])=[O:9])=[C:6]([NH:14][CH3:15])[N:5]([C:19]2[C:24]([Cl:25])=[CH:23][C:22]([C:26]([F:29])([F:28])[F:27])=[CH:21][C:20]=2[Cl:30])[N:4]=1)#[N:2]

参加物

5

反応物 3

HCID 176Acetic AcidHCID 4311764Sodium borohydride2 回HCID 572956413-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxymethylideneamino-4-trifluoromethylsulfinylpyrazole

生成物 1

HCID 229883203-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-methylamino-4-trifluoromethylsulfonylpyrazole収率 22.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
10 °C

実験手順

A 50 L reactor was charged with 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxymethylideneamino-4-trifluoromethylsulfinylpyrazole (1.645 g, 3.335 moles) and absolute ethanol (16 L) under nitrogen. The solution was cooled to 10° C., and sodium borohydride (266 g, 7.03 moles) was added slowly such that the temperature remained generally below 35° C. After 6.75 h, some additional sodium borohydride (25 g, 0.66 mole) was added and stirring was continued overnight. Acetic acid (1.3 L, 22.7 moles) was added to quench, followed by 16 L of water. The resulting precipitate was collected by filtration, washed with water, and air-dried. Recrystallization from methanol afforded 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-methylamino-4-trifluoromethylsulfonylpyrazole (350 g) as an off-white solid (m.p. about 227° C.).

後処理

  1. customremained generally below 35° C
  2. waitwas continued overnight
  3. customto quench
  4. filtrationThe resulting precipitate was collected by filtration
  5. washwashed with water
  6. customair-dried
  7. customRecrystallization from methanol

出典と根拠

ORDレコード
ord-0c0a6119baaf48b08780ade78c6993a1
出典データセット
uspto-grants-2003_10
特許番号
US06630499B1

反応ノート

読み込み中…