Potassium Carbonate → 3,4-Bis(2,2,2-trifluoroethoxy)nitrobenzene

HRID 2412332ノート

反応式

HRID 2412332 の反応式
[C:1](=[O:4])([O-])[O-].[K+].[K+].FC(F)(F)S([O:12][CH2:13][C:14]([F:17])([F:16])[F:15])(=O)=O.[N+:20]([C:23]1[CH:24]=[C:25](O)[C:26](=[CH:28][CH:29]=1)O)([O-:22])=[O:21]>CC(C)=O>[F:17][C:14]([F:15])([F:16])[CH2:13][O:12][C:28]1[CH:29]=[C:23]([N+:20]([O-:22])=[O:21])[CH:24]=[CH:25][C:26]=1[O:4][CH2:1][C:14]([F:17])([F:16])[F:15]

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 803662,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 35051094-Nitrocatechol

生成物 1

HCID 133704333,4-Bis(2,2,2-trifluoroethoxy)nitrobenzene

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

To a refluxing mixture of 12.7 g (0.092 mole) of potassium carbonate, 21.3 g. (0.092 mole) of 2,2,2-trifluoroethyl trifluoromethanesulfonate and 62 ml. of acetone is added dropwise 6.2 g. (0.040 mole) of 4-nitrocatechol in 62 ml. of acetone over about 2.5 hours. Refluxing is continued for a total of 24 hours, then the solution is evaporated. The residue is mixed with equal volumes of water and diethyl ether. The ether layer is separated, washed with water and saturated sodium chloride solution and dried. Evaporation provides crude 3,4-bis(2,2,2-trifluoroethoxy)nitrobenzene. Chromatographic purification on a silica gel column is effected by eluting with mixtures of chloroform and hexane. Recrystallization from cyclohexane with a small amount of benzene provides solid product, m.p. 63°-65° C.

後処理

  1. temperatureRefluxing
  2. customis continued for a total of 24 hours
  3. customthe solution is evaporated
  4. additionThe residue is mixed with equal volumes of water and diethyl ether
  5. customThe ether layer is separated
  6. washwashed with water and saturated sodium chloride solution
  7. customdried
  8. customEvaporation

出典と根拠

ORDレコード
ord-a2c1c22ccc03492188752860682324a1
出典データセット
uspto-grants-1985_01
特許番号
US04491584

反応ノート

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