Ammonia → Flunamine

HRID 1415173

反応式

HRID 1415173 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[O:9][CH2:10][CH2:11]Cl)=[CH:4][CH:3]=1.[NH3:20].O>CO>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[O:9][CH2:10][CH2:11][NH2:20])=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 222AmmoniaHCID 962WaterHCID 107793021-[Bis(4-fluorophenyl)methoxy]-2-chloroethane

生成物 1

HCID 39658Flunamine収率 58.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
135 °C

実験手順

A mixture of 28.2 g (0.1 mole) of 2-[bis(p-fluorophenyl)methoxy]ethyl chloride and 17 g (1 mole) of ammonia in 187.5 ml of methanol is shaken in an autoclave for a period of 6 hours at 135° C. The reaction mixture is poured into water and extracted with diethyl ether. The extract is acidified with 2N hydrochloric acid. The acid aqueous layer is separated off, made alkaline with 2N sodium hydroxide and extracted with diethyl ether. The extract is dried over potassium carbonate and the ether is distilled off. The residue is distilled, yielding 15.4 g of 2-[bis(p-fluorophenyl)-methoxy]ethylamine, boiling point 130° C/0.2 mm.Hg. The base is dissolved in diethyl ether and an ethereal solution of maleic acid is added. The precipitate is filtered off and crystallised from a mixture of ethanol and diethyl ether. 2-[Bis(p-fluorophenyl)methoxy]ethylamine hydrogen maleate is obtained. Its melting point is 126°-127° C.

後処理

  1. extractionextracted with diethyl ether
  2. customThe acid aqueous layer is separated off
  3. extractionextracted with diethyl ether
  4. dry with materialThe extract is dried over potassium carbonate
  5. distillationthe ether is distilled off
  6. distillationThe residue is distilled

出典と根拠

ORDレコード
ord-7222a985963d4f8f942530c17e6e65a0
出典データセット
uspto-grants-1977_01
特許番号
US04003932

関連ノート

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