Acetone → HCID 21319892, 화합물

HRID 1703554노트

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HRID 1703554 반응식
Br[CH2:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([N+:11]([O-:13])=[O:12])=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:7]=2[CH:20]=1.CC(C)=O.C(O)C.[C-:28]#[N:29].[Na+]>O>[C:28]([CH2:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([N+:11]([O-:13])=[O:12])=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:7]=2[CH:20]=1)#[N:29]

참가 물질

6

반응물 4

HCID 180AcetoneHCID 702EthanolHCID 8929Sodium CyanideHCID 13531604HCID 13531604, 화합물

생성물 1

HCID 21319892HCID 21319892, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 5-bromomethyl-2-nitro-3-phenylbenzofuran (5 g., 0.015 mole) in 95 ml. of acetone is treated with 20 ml. of ethanol, and the mixture is heated to its reflux temperature. To this mixture is added 0.015 mole of sodium cyanide dissolved in 9 ml. of water, and refluxing is continued for about two hours. The mixture is evaporated under vacuum, then dichloromethane and water are added to the residue. The organic layer is separated, washed with water and dried. The organic layer is then evaporated under vacuum. The residue is purified by eluting twice with benzene through a silica gel column, followed by refluxing in 30 ml. of diethyl ether. The yellow precipitate is separated by filtration and recrystallized twice from benzene to provide 5-cyanomethyl-2-nitro-3-phenylbenzofuran, m.p. 166°-168° C.

후처리

  1. temperaturereflux temperature
  2. dissolutiondissolved in 9 ml
  3. customThe mixture is evaporated under vacuum
  4. additiondichloromethane and water are added to the residue
  5. customThe organic layer is separated
  6. washwashed with water
  7. customdried
  8. customThe organic layer is then evaporated under vacuum
  9. customThe residue is purified
  10. washby eluting twice with benzene through a silica gel column
  11. temperatureby refluxing in 30 ml
  12. customThe yellow precipitate is separated by filtration
  13. customrecrystallized twice from benzene

출처 및 근거

ORD 기록
ord-e89899309aee4bd7b12f0b22e07bc5b0
출처 데이터셋
uspto-grants-1978_11
특허 번호
US04124704

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