1,3(2H)-Pyridinedicarboxylic acid, 5,6-dihydro-, 1-(1,1-dimethylethyl) ester - Names and Identifiers
Name | 1-(tert-butoxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid
|
Synonyms | LogP 1-Boc-1,2,5,6-tetrahydropyridine-3-carboxylic acid 1-(tert-butoxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxylic acid 1-[(tert-butoxy)carbonyl]-1,2,5,6-tetrahydropyridine-3-carboxylic acid 1,3(2H)-Pyridinedicarboxylic acid, 5,6-dihydro-, 1-(1,1-dimethylethyl) ester 1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2h-pyridine-5-carboxylic Acid
|
CAS | 86447-11-2
|
InChI | InChI=1/C11H17NO4/c1-11(2,3)16-10(15)12-6-4-5-8(7-12)9(13)14/h5H,4,6-7H2,1-3H3,(H,13,14) |
1,3(2H)-Pyridinedicarboxylic acid, 5,6-dihydro-, 1-(1,1-dimethylethyl) ester - Physico-chemical Properties
Molecular Formula | C11H17NO4
|
Molar Mass | 227.26 |
Density | 1.207g/cm3 |
Boling Point | 356.942°C at 760 mmHg |
Flash Point | 169.673°C |
Vapor Presure | 0mmHg at 25°C |
Storage Condition | 2-8°C |
Refractive Index | 1.519 |
1,3(2H)-Pyridinedicarboxylic acid, 5,6-dihydro-, 1-(1,1-dimethylethyl) ester - Introduction
1-(tert-butoxycarbonyl)-1,2,5, acid, also known as 1-(tert-butoxycarbonyl)-1,2,5, acid, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 1-(tert-butoxycarbonyl)-1,2,5, acrylic is a colorless to light yellow solid.
-Solubility: It has good solubility in organic solvents such as acetone, dimethylformamide and dichloromethane.
Use:
- 1-(tert-butoxycarbonyl)-1,2,5, acid is a commonly used reagent in the field of organic synthesis and can be used to synthesize other compounds.
-It is often used as a reagent to protect the hydroxyl group (OH), by reacting it with the hydroxyl group to form an ester, thereby protecting the hydroxyl group from other reactions.
Preparation Method:
- 1-(tert-butoxycarbonyl)-1,2,5,-acid is usually synthesized by the following steps:
1.1,2,5,6-tetrahydropyridine is reacted with sodium hydroxide to obtain 1,2,5,6-tetrahydropyridine sodium salt.
2.1,2,5,6-tetrahydropyridine sodium salt is reacted with tert-butyl carbonate to obtain 1-BOC-1,2,5, 6-tetrahydropyridine.
3. Finally, 1-BOC-1,2,5,6-tetrahydropyridine is reacted with anhydrous tert-butanol acid to obtain 1-(tert-butoxycarbonyl)-1,2,5, pyridoxide.
Safety Information:
- 1-(tert-butoxycarbonyl)-1,2,5, acrylic belongs to chemicals and needs to be operated in chemical laboratories.
-During operation, wear appropriate personal protective equipment, such as lab gloves and goggles, to avoid contact with skin, eyes and respiratory system.
-Avoid inhaling its dust or mist and ensure that it is used in a well-ventilated place.
-When storing, keep it in a sealed container, away from fire and oxidizing agents, and avoid high temperatures.
Last Update:2024-04-09 21:00:56