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Dicyclohexylcarbodiimide → Methyl 8-(Boc-amino)-octanoate

HRID 975792
ノート
印刷プレビュー

反応式

HRID 975792 の反応式
[C:1]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[CH2:19]1CCC(N=C=NC2CCCCC2)CC1>CO>[C:1]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([O:18][CH3:19])=[O:17])([O:3][C:4]([CH3:6])([CH3:7])[CH3:5])=[O:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10868DicyclohexylcarbodiimideHCID 5462158-(((Tert-butoxy)carbonyl)amino)octanoic acid

生成物 1

HCID 130187773Methyl 8-(Boc-amino)-octanoate収率 79%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

BocNH(CH2)7CO2H (prepared, Example 8, Step 1) (300 mg, 1.2 mmol) was dissolved in methanol (5 mL) and DCC (239 mg, 1.2 mmol) was then added. The solution was stirred at room temperature overnight. The DCU was removed by filtration and the solvent was removed in vacuo. The residue was then taken up in EtoAc and washed with dilute HCl (200 mL×3), water (200 mL×3), and then dried over MgSO4, filtered, and the solvent was removed in vacuo to yield an oil, 0.259 g (79% yield);

後処理

  1. customThe DCU was removed by filtration
  2. customthe solvent was removed in vacuo
  3. washwashed with dilute HCl (200 mL×3), water (200 mL×3)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customthe solvent was removed in vacuo
  7. customto yield an oil, 0.259 g (79% yield)

出典と根拠

ORDレコード
ord-e39aaf1e6658456e926d5b8e55b18cde
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05610145

反応ノート

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