4-Bromo-1,1,2-trifluorobut-1-ene → 3,4,4-Trifluoro-3-butenyl dithiocarbamate

HRID 132092

反応式

HRID 132092 の反応式
[C:1](=[S:4])([S-:3])[NH2:2].[NH4+].Br[CH2:7][CH2:8][C:9]([F:13])=[C:10]([F:12])[F:11]>C(O)C>[C:1](=[S:3])([S:4][CH2:7][CH2:8][C:9]([F:13])=[C:10]([F:12])[F:11])[NH2:2]

参加物

4

反応条件

温度
40 °C

実験手順

2.8 g (25 mmol) of ammonium dithiocarbamate in 40 ml of ethanol are admixed dropwise with 5.32 g (26.3 mmol; purity 93.2%) of 4-bromo-1,1,2-trifluoro-1-butene, stirred at 40° C. for 3 h, another 2.8 g of ammonium dithiocarbamate is added after 1 h, and everything is left to stand at room temperature for 8 h. The filtrate is filtered off with suction and concentrated by evaporation under reduced pressure, the residue taken up in dichloromethane and washed once with water, and the organic phase dried over sodium sulphate. After concentration by evaporation under reduced pressure, 4.3 g (63% of theory; purity by GC/MS: 74 area %) of a semicrystalline residue are obtained.

後処理

  1. waiteverything is left
  2. waitto stand at room temperature for 8 h
  3. filtrationThe filtrate is filtered off with suction
  4. concentrationconcentrated by evaporation under reduced pressure
  5. washwashed once with water
  6. dry with materialthe organic phase dried over sodium sulphate
  7. concentrationAfter concentration
  8. customby evaporation under reduced pressure, 4.3 g (63% of theory; purity by GC/MS: 74 area %) of a semicrystalline residue
  9. customare obtained

出典と根拠

ORDレコード
ord-09ca7a1c3a124903bbd1d02c670913c3
出典データセット
uspto-grants-2008_06
特許番号
US07385093B2

関連ノート

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