Dichloromethane → 4-[[3-(p-Chlorophenyl)propyl]methylamino]benzoic acid, ethyl ester

HRID 1154354

反応式

HRID 1154354 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][NH:11][C:12]2[CH:22]=[CH:21][C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:14][CH:13]=2)=[CH:4][CH:3]=1.Cl[CH2:24]Cl.CS(F)(=O)=O.[OH-].[Na+]>O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][N:11]([CH3:24])[C:12]2[CH:13]=[CH:14][C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:21][CH:22]=2)=[CH:6][CH:7]=1

参加物

6

反応物 4

HCID 6344DichloromethaneHCID 11207Methanesulfonyl FluorideHCID 14798Sodium HydroxideHCID 13079692Ethyl 4-{[3-(4-chlorophenyl)propyl]amino}benzoate

生成物 1

HCID 442788874-[[3-(p-Chlorophenyl)propyl]methylamino]benzoic acid, ethyl ester

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 1.0 g. of ethyl 4-[3-(p-chlorophenyl)propylamino]benzoate, 20 ml. of dry dichloromethane and 2.5 ml. of methane sulfonyl fluoride is stirred for 18 hours, then refluxed for 3 hours. The solution is poured into 30 ml. of water and adjusted to pH 10 with 10N sodium hydroxide. The dichloromethane layer is separated and saved. The aqueous layer is extracted with two 20 ml. portions of dichloromethane. The organic layers are combined, washed with 10 ml. of water, dried over anhydrous magnesium sulfate, and evaporated to yield 1.80 g. of the desired product as a light yellow oil.

後処理

  1. additionA mixture of 1.0 g
  2. temperaturerefluxed for 3 hours
  3. additionThe solution is poured into 30 ml
  4. customThe dichloromethane layer is separated
  5. extractionThe aqueous layer is extracted with two 20 ml
  6. washwashed with 10 ml
  7. dry with materialof water, dried over anhydrous magnesium sulfate
  8. customevaporated
  9. customto yield 1.80 g

出典と根拠

ORDレコード
ord-fece9dcecc9d4259b9318987b022f9b8
出典データセット
uspto-grants-1984_12
特許番号
US04489094

関連ノート

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