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Dicyclohexylcarbodiimide → Ethyl 4-(2-(11-Bromoundecanoylamino)phenoxy)-butyrate

HRID 1290714
ノート
印刷プレビュー

反応式

HRID 1290714 の反応式
[NH2:1][C:2]1[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9].[Br:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][C:28](O)=[O:29].C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl.CN(C)C1C=CN=CC=1>[Br:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][C:28]([NH:1][C:2]1[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10868DicyclohexylcarbodiimideHCID 1781211-Bromoundecanoic acidHCID 11816929Ethyl 4-(2-aminophenoxy)butanoate

生成物 1

HCID 19603128Ethyl 4-(2-(11-Bromoundecanoylamino)phenoxy)-butyrate収率 50%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒
HCID 6344
Dichloromethane
溶媒

実験手順

To a solution of (4) (2.60 g., 11 mM) and 11-bromoundecanoic acid (2.65 g., 10 mM) in anhydrous methylene chloride (90 mL) is added 4-(dimethylamino)pyridine (1.22 g., 10 mM) followed by N,N'-dicyclohexylcarbodiimide (2.3 g., 11 mM) (4×5 mL of methylenechloride rinses). Precipitation of dicyclohexylurea (DCU) begins within 4 minutes. When TLC analysis indicates the reaction is complete, the mixture is filtered, the filtrate concentrated in vacuo and the residue extracted with ether. The combined ether extracts are washed 1× with 1N hydrochloric acid, 1× saturated sodium chloride solution, dried (Na2SO4) and concentrated to a residue which is stirred, filtered, and concentrated alternately with ether and methylene chloride until all DCU is removed. Concentration of the final solution yields the title product (32) (2.35 g.) as an oil that goes readily to a waxy solid.

後処理

  1. customPrecipitation of dicyclohexylurea (DCU)
  2. filtrationthe mixture is filtered
  3. concentrationthe filtrate concentrated in vacuo
  4. extractionthe residue extracted with ether
  5. washThe combined ether extracts are washed 1× with 1N hydrochloric acid, 1× saturated sodium chloride solution
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated to a residue which
  8. filtrationfiltered
  9. concentrationconcentrated alternately with ether and methylene chloride until all DCU
  10. customis removed

出典と根拠

ORDレコード
ord-b10d6fcb4475433f919013e6dd75d2a3
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05753641

反応ノート

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