Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Basic information
- Product Name:
- Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
- Synonyms:
-
- Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
- Nsc145143
- cis-Methyl 4-aMinocyclohexanecarboxylate hydrochloride
- cis-4-amino-cyclohexanecarboxylic methyl ester, hydrochloride
- Methyl cis-4-aminocyclohexanecarboxylate HCl
- H-1,4-cis-ACHC-OMe Hydrochloride
- Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
- (1S,4S)-Methyl 4-aminocyclohexanecarboxylate hydrochloride
- CAS:
- 61367-16-6
- MF:
- C8H15NO2.ClH
- MW:
- 193.672
- Mol File:
- 61367-16-6.mol
Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Chemical Properties
- Melting point:
- 188°C(lit.)
- storage temp.
- Inert atmosphere,Room Temperature
- form
- powder to crystal
- color
- White to Almost white
Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Usage And Synthesis
Chemical Properties
White crystalline powder
Uses
Methyl cis-4-aminocyclohexanecarboxylate HCl
Synthesis
67-56-1
1776-53-0
61367-07-5
Step A: Preparation of methyl trans-4-aminocyclohexanecarboxylate hydrochloride. Trans-4-aminocyclohexanecarboxylic acid (200 mg, 1.40 mmol) was suspended in methanol (5.5 mL) and cooled to -10 °C. Thionyl chloride (204 μL, 2.79 mmol) was added dropwise under stirring and the reaction mixture was stirred at -10 °C for 15 min. Subsequently, the reaction system was slowly warmed to room temperature and stirring was continued for 15 min, after which it was heated to reflux for 1 hr. After completion of the reaction, the reaction was cooled to room temperature and the reaction mixture was concentrated under reduced pressure to afford the white solid product methyl trans-4-aminocyclohexanecarboxylate hydrochloride (260 mg, 96.1% yield). Mass spectral analysis (APCI) showed m/z = 158.0 ([M+H]+).
References
[1] Patent: WO2011/6074, 2011, A1. Location in patent: Page/Page column 95
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