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1-(Phenylmethyl) butanedioate → Benzyl (Chloromethyl) Succinate

HRID 489000
ノート
印刷プレビュー

反応式

HRID 489000 の反応式
[CH2:1]([O:8][C:9](=[O:15])[CH2:10][CH2:11][C:12]([OH:14])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].C([N+](CCCC)(CCCC)CCCC)CCC.[Cl:34][CH2:35]I>O1CCOCC1>[Cl:34][CH2:35][O:13][C:12](=[O:14])[CH2:11][CH2:10][C:9]([O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 87881-(Phenylmethyl) butanedioateHCID 11644ChloroiodomethaneHCID 2723671Tetrabutylammonium Hydroxide

生成物 1

HCID 10801108Benzyl (Chloromethyl) Succinate

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Succinic acid monobenzyl ester (4.16 g, 20 mmole) was dissolved in dioxane (20 ml). To the solution was added tetrabutylammonium hydroxide aqueous solution (40%, 11.6 ml, 18 mmole). The solution was dried in vacuo and coevaporated with toluene several times. The residue was dissolved in methylene chloride (60 ml) and then chloroiodomethane (14.5 ml, 200 mmole) was added to the solution. The reaction solution was stirred for 18 hr and then evaporated and the product was isolated with silica gel column chromatography. 3.64 g

後処理

  1. customThe solution was dried in vacuo
  2. dissolutionThe residue was dissolved in methylene chloride (60 ml)
  3. customevaporated
  4. customthe product was isolated with silica gel column chromatography

出典と根拠

ORDレコード
ord-3fa9c7eeaad84eba9cefb08f5d4cd58f
出典データセット
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06974802B2

反応ノート

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