ChemicalBook--->CAS DataBase List--->215597-35-6

215597-35-6

215597-35-6 Structure

215597-35-6 Structure
IdentificationBack Directory
[Name]

1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
[CAS]

215597-35-6
[Synonyms]

1, 1-ACCB(OME)
Methyl 1-aMinocyclobutanecarboxylate
methyl 1-aminocyclobutane-1-carboxylate
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER
Cyclobutanecarboxylic acid, 1-aMino-, Methyl ester
Cyclobutanecarboxylic acid, 1-amino-, methyl ester (9CI)
1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER USP/EP/BP
Cyclobutanecarboxylicacid, 1-amino-, methyl ester, hydrochlo...
[Molecular Formula]

C6H11NO2
[MDL Number]

MFCD01318265
[MOL File]

215597-35-6.mol
[Molecular Weight]

129.16
Chemical PropertiesBack Directory
[Boiling point ]

162.3±23.0 °C(Predicted)
[density ]

1.127±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

Solid
[pka]

7.71±0.20(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
Spectrum DetailBack Directory
[Spectrum Detail]

1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER(215597-35-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

N-Boc-1-aminocyclobutanecarboxylic acid

120728-10-1

1-AMINO-CYCLOBUTANECARBOXYLIC ACID METHYL ESTER

215597-35-6

Stage 1: Synthesis of methyl 1-aminocyclobutanecarboxylate Concentrated H2SO4 (10 ml) was slowly added to a methanol solution (30 ml) containing 1-(tert-butoxycarbonylamino)-cyclobutane-1-carboxylic acid (9.29 mmol, 1 eq.) at 0°C. The reaction mixture was refluxed at 0°C for 2 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in distilled water and the pH was adjusted to 8-9 with saturated sodium bicarbonate solution, followed by extraction with ethyl acetate (2 x 200 ml). The combined organic phases were washed sequentially with distilled water (2 x 150 ml) and saturated NaCl solution (2 x 50 ml) and dried with anhydrous sodium sulfate. Finally, the solvent was removed by concentration under reduced pressure to afford methyl 1-aminocyclobutanecarboxylate as a white solid in 75% yield.

[References]

[1] Patent: US2010/173889, 2010, A1. Location in patent: Page/Page column 34
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