TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER
TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Basic information
- Product Name:
- TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER
- Synonyms:
-
- TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER
- (trans-4-Carboethoxycyclohexyl)amine
- Ethyl trans-4-Aminocyclohexanecarboxylate
- Cyclohexanecarboxylicacid,4-aMino-,ethylester,trans-
- (1s,4s)-ethyl 4-aminocyclohexanecarboxylate
- trans-Ethyl 4-aminocyclohexanecarboxylate
- Ethyl trans-4-aminocyclohexane-1-carboxylate
- CAS:
- 1678-68-8
- MF:
- C9H17NO2
- MW:
- 171.24
- Product Categories:
-
- Chemical Amines
- Amines
- Mol File:
- 1678-68-8.mol
TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Chemical Properties
- Boiling point:
- 139-140℃ (13 Torr)
- Density
- 1.018±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 10.36±0.70(Predicted)
- Appearance
- Light yellow to yellow Liquid
TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Usage And Synthesis
Chemical Properties
Yellow Solid
Synthesis
64-17-5
27960-59-4
1678-68-8
General procedure for the synthesis of ethyl trans-4-aminocyclohexanecarboxylate from ethanol and trans-4-aminocyclohexanecarboxylic acid hydrochloride: 1. concentrated hydrochloric acid (7 mL) was added to a suspension of (1r,4r)-4-aminocyclohexanecarboxylic acid hydrochloride (6.32 g, 0.035 mol) in ethanol (100 mL) and the mixture was stirred. 2. The mixture was heated to 60 °C and the reaction was kept overnight. 3. Upon completion of the reaction, the mixture was evaporated under vacuum to remove the solvent. 4. The residue was thoroughly removed from water by azeotropy with water, followed by azeotropy with ethanol and finally azeotropy with toluene to afford the title product ethyl trans-4-aminocyclohexanecarboxylate as a white solid (7.2 g, 98% yield). 5. The structure of the product was determined by 1H2O2 analysis. 5. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 4.05 (q, J = 7.1 Hz, 2H), 2.95 (bs, 1H), 2.30-2.15 (m, 1H), 2.02-1.88 (m, 4H), 1.43-1.28 (m, 4H), 1.22-1.13 (t, J = 6.9 Hz, 3H). Hz, 3H).
References
[1] Patent: WO2016/46390, 2016, A1. Location in patent: Page/Page column 44
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 22, p. 9199 - 9221
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