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HRID1383251

反应详情

EQUATION

反应方程式

HRID 1383251 的结构方程式

REACTANTS

反应物

2
结构：O=C(O)CC(O)(CC(=O)O)C(=O)O
HCID311

Citric acid

C6H8O7

结构：CC1(C)CC(O)CC(C)(C)N1O
HCID5395

1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine

C9H19NO2

PRODUCTS

生成物

1
结构：CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
HCID22182978

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

1
结构：O
溶剂HCID962

Water

H2O

PROCEDURE

实验过程

To a glass 0.5 L reaction bottle are added 20.0 g (116 mmol) of 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine, 22.2 g (116 mmol) citric acid, 200 mg 5% Pt on C and 100 mL water. Catalytic hydrogenation is carried out at 50 psi for 30 minutes at room temperature. Catalyst is removed by filtration through a pad of Celite. The aqueous salt solution has a pH of 3.30. Removal of water yields the product as a hygroscopic glassy solid.

WORKUP

后处理

  1. customCatalyst is removed by filtration through a pad of Celite
  2. customRemoval of water