4-Methylbenzylamine → 2,2-difluoro-N-(4-methylbenzyl)ethanamine

HRID 2098415ノート

反応式

HRID 2098415 の反応式
[F:1][CH:2]([F:5])[CH2:3]Cl.[CH3:6][C:7]1[CH:14]=[CH:13][C:10]([CH2:11][NH2:12])=[CH:9][CH:8]=1>O>[F:1][CH:2]([F:5])[CH2:3][NH:12][CH2:11][C:10]1[CH:13]=[CH:14][C:7]([CH3:6])=[CH:8][CH:9]=1

参加物

4

反応物 2

HCID 660354-Methylbenzylamine2 回HCID 2736499Chlorodifluoroethane (mixed isomers)

生成物 1

HCID 609230682,2-difluoro-N-(4-methylbenzyl)ethanamine収率 58%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

An amount of 26.2 g (242 mmol) of 2,2-difluoro-1-chloroethane and 10 g of 4-methylbenzylamine (80.8 mmol) are heated in an autoclave at an internal temperature of 120° C. for 16 hours. Subsequently, 50 g of water are added and the aqueous phase is separated. The aqueous phase is again extracted with 2,2-difluoro-1-chloroethane and the combined organic phases are distilled as described in Example 1.1. Here also, the 4-methylbenzylamine hydrochloride which is present in the aqueous phase can be converted back into free 4-methylbenzylamine by addition of sodium hydroxide solution. After distillation, 4.3 g of 2,2-difluoro-N-(4-methylbenzyl)ethanamine are obtained, which corresponds to a yield of 58%, based on reacted 4-methylbenzylamine.

後処理

  1. customthe aqueous phase is separated
  2. extractionThe aqueous phase is again extracted with 2,2-difluoro-1-chloroethane
  3. distillationthe combined organic phases are distilled
  4. additioncan be converted back into free 4-methylbenzylamine by addition of sodium hydroxide solution
  5. distillationAfter distillation, 4.3 g of 2,2-difluoro-N-(4-methylbenzyl)ethanamine
  6. customare obtained

出典と根拠

ORDレコード
ord-a9015e25fd45480f8288826f21702d51
出典データセット
uspto-grants-2013_05
特許番号
US08450528B2

反応ノート

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