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盐酸 → 6-[(tert-butoxy)carbonyl]-6-azaspiro[2.5]octane-5-carboxylic acid

HRID 712787
笔记
打印预览

反应方程式

HRID 712787 反应方程式
[C:1]([O:5][C:6]([N:8]1[CH2:15][CH2:14][C:11]2([CH2:13][CH2:12]2)[CH2:10][CH:9]1[C:16]([O-:18])=[O:17])=[O:7])([CH3:4])([CH3:3])[CH3:2].C([NH2+]C(C1C=CC=CC=1)C)C1C=CC=CC=1.Cl.[Na+].[Cl-]>CCOC(C)=O>[C:1]([O:5][C:6]([N:8]1[CH2:15][CH2:14][C:11]2([CH2:12][CH2:13]2)[CH2:10][CH:9]1[C:16]([OH:18])=[O:17])=[O:7])([CH3:4])([CH3:2])[CH3:3]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 313盐酸HCID 5234Halite (NaCl)HCID 89350970N-benzyl-1-phenylethanaminium 6-(tert-butoxycarbonyl)-6-azaspiro[2.5]octane-5-carboxylate

产物 1

HCID 711873446-[(tert-butoxy)carbonyl]-6-azaspiro[2.5]octane-5-carboxylic acid收率 81.6%

试剂、催化剂与溶剂 1

HCID 8857乙酸乙酯溶剂

反应条件

温度
0 °C

实验过程

To a suspension of N-benzyl-1-phenylethanaminium 6-(tert-butoxycarbonyl)-6-azaspiro[2.5]octane-5-carboxylate (single unknown enantiomer) (D2) (10 g, 24 mmol) in EtOAc (100 mL) stirred at 0° C. was slowly added aqueous HCl 0.5N (100 ml) saturated with NaCl. After addition was completed, dissolution was observed. The organic layer was decanted, washed with saturated NaCl, dried (Na2SO4) and evaporated in vacuo to afford 5 g of acid which was recrystallized from petroleum ether/EtOAc (60 ml/20 ml) to afford the tile compound (D3) (2.8 g) as white solid.

后处理

  1. additionAfter addition
  2. dissolutiondissolution
  3. customThe organic layer was decanted
  4. washwashed with saturated NaCl
  5. dry with materialdried (Na2SO4)
  6. customevaporated in vacuo

来源与证据

ORD记录
ord-86ce547e21c143ecabd0b449ec26e602
来源数据集
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
专利号
US09181279B2

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记