ChemicalBook--->CAS DataBase List--->51498-33-0

51498-33-0

51498-33-0 Structure

51498-33-0 Structure
IdentificationBack Directory
[Name]

4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER
[CAS]

51498-33-0
[Synonyms]

Ethyl 4-aMinocyclohexanecarboxylate
4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER
Cyclohexanecarboxylic acid, 4-aMino-, ethyl ester
[Molecular Formula]

C9H17NO2
[MDL Number]

MFCD01995051
[MOL File]

51498-33-0.mol
[Molecular Weight]

171.24
Chemical PropertiesBack Directory
[Boiling point ]

114-117 °C(Press: 10 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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Synthesis]

4-AMINOCYCLOHEXANECARBOXYLIC ACID

1776-53-0

Ethanol

64-17-5

4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER

51498-33-0

GENERAL STEPS: 4-Aminocyclohexanecarboxylic acid (5.0 g, 34.92 mmol) was dissolved in ethanol (20 mL) and cooled to 0 °C. Thionyl chloride (7.60 mL, 104.76 mmol) was slowly added dropwise with stirring. After the dropwise addition, the reaction mixture was heated to 80 °C and maintained for 2-3 hours. The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the solvent was removed by evaporation under reduced pressure to give ethyl 4-aminocyclohexane-1-carboxylate in quantitative yield.

[References]

[1] Patent: US2012/88750, 2012, A1. Location in patent: Page/Page column 41
[2] Patent: WO2006/77424, 2006, A1. Location in patent: Page/Page column 162-163
[3] Patent: WO2006/77425, 2006, A1. Location in patent: Page/Page column 162-163
[4] Patent: WO2006/77428, 2006, A1. Location in patent: Page/Page column 140
[5] Patent: US2013/252938, 2013, A1. Location in patent: Paragraph 0502
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