Dimethylformamide → Trans-beta-dimethylamino-4-methyl-2-nitrostyrene

HRID 1390844

反応式

HRID 1390844 の反応式
[N+:1]([C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:5]=1[CH3:11])([O-:3])=[O:2].CO[CH:14](OC)[N:15]([CH3:17])[CH3:16].CN(C)C=O>CO>[CH3:14][N:15]([CH3:17])/[CH:16]=[CH:11]/[C:5]1[CH:6]=[CH:7][C:8]([CH3:10])=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2]

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 6974Nitro-p-xyleneHCID 78373Dimethylformamide dimethyl acetal

生成物 1

HCID 20550574Trans-beta-dimethylamino-4-methyl-2-nitrostyrene収率 83%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

A 12-l. three-necked flask, equipped with a thermometer, a mechanical stirrer and a 60 cm. vacuum-jacketed silvered column with glass helice packing connected to a total-condensation, variable take-off still head with receiver was charged under nitrogen with 675 g (4.46 moles) of 2-nitro-1,4-dimethylbenzene, 736 g (6.17 moles) of N,N-dimethyl formamide dimethyl acetal and 3.0 l of N,N-dimethylformamide. The mixture was stirred and heated with a heating mantle for 37 hours. The pot temperature was gradually raised from 130° to 144° while the formed methanol was removed by distillation. The fractionating column was replaced by a distilling head with condenser and receiver (cooled in a dry ice-acetone bath). The dimethylformamide was removed by distillation, first at aspirator vacuum and then at high vacuum (water bath 70°), giving a residue of 924 g (100%) of crude product as a dark red viscous oil. This material was poured into a beaker and mixed thoroughly with 640 ml of methyl alcohol. The mixture was stirred in an ice bath until the product crystallized in mass and was then refrigerated overnight. The precipitate was collected by suction filtration, washed with 320 ml of methyl alcohol and dried in vacuo at room temperature (constant weight) to afford 760 g (83%) of product as a free-flowing, dark-red crystalline solid, m.p. 41.5-43.5° C.

後処理

  1. customthree-necked flask, equipped with a thermometer, a mechanical stirrer
  2. customvacuum-jacketed silvered column with glass helice packing connected to a total-condensation, variable take-off still head with receiver
  3. temperatureheated with a heating mantle for 37 hours
  4. customwas removed by distillation
  5. customThe fractionating column was replaced by a distilling head with condenser
  6. temperaturereceiver (cooled in a dry ice-acetone bath)
  7. customThe dimethylformamide was removed by distillation, first at aspirator vacuum
  8. customat high vacuum (water bath 70°), giving a residue of 924 g (100%) of crude product as a dark red viscous oil
  9. additionThis material was poured into a beaker
  10. stirringThe mixture was stirred in an ice bath until the product
  11. customcrystallized in mass
  12. customrefrigerated overnight
  13. filtrationThe precipitate was collected by suction filtration
  14. washwashed with 320 ml of methyl alcohol
  15. customdried in vacuo at room temperature (constant weight)

出典と根拠

ORDレコード
ord-ad3137969d3f4ef8a34cc61a309c947a
出典データセット
uspto-grants-1979_02
特許番号
US04140697

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