ChemicalBook--->CAS DataBase List--->107259-05-2

107259-05-2

107259-05-2 Structure

107259-05-2 Structure
IdentificationBack Directory
[Name]

SINOVA SL-03967
[CAS]

107259-05-2
[Synonyms]

SINOVA SL-03967
Ethyl 1-(Boc-aMino)cyclopropanecarboxylate
1-N-(BOC)AMino-cyclopropane-1-carboxylic acid ethyl ester
Ethyl 1-((tert-butoxycarbonyl)aMino)cyclopropanecarboxylate
ethyl 1-((tert-butoxycarbonyl)amino)cyclopropane-1-carboxylate
Ethyl 1-[(2-methylpropan-2-yl)oxycarbonylamino]cyclopropane-1-carboxylate
1-[[(1,1-dimethylethoxy)carbonyl]amino]Cyclopropane carboxylic acid Ethyl ester
Cyclopropanecarboxylic acid, 1-[[(1,1-diMethylethoxy)carbonyl]aMino]-, ethyl ester
[Molecular Formula]

C11H19NO4
[MDL Number]

MFCD11845623
[MOL File]

107259-05-2.mol
[Molecular Weight]

229.27
Chemical PropertiesBack Directory
[Melting point ]

44-46 °C(Solv: pentane (109-66-0))
[Boiling point ]

307.0±21.0 °C(Predicted)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

10.87±0.20(Predicted)
[Appearance]

White to off-white Solid
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

Ethyl 1-aminocyclopropanecarboxylate hydrochloride

42303-42-4

SINOVA SL-03967

107259-05-2

The general procedure for the synthesis of ethyl 1-(BOC-amino)cyclopropane-1-carboxylate from di-tert-butyl dicarbonate and ethyl 1-aminocyclopropane-1-carboxylate hydrochloride was as follows: to a solution of 1-aminocyclopropane carboxylic acid ethyl ester hydrochloride (3.22 g, 19.4 mmol) in dichloromethane (35 mL) was added triethylamine (2.71 mL, 19.4 mmol) to form a suspension. A solution of dichloromethane (5 mL) of di-tert-butyl dicarbonate (4.24 g, 19.4 mmol) was added slowly and dropwise over about 5 hours. The reaction mixture was stirred overnight at room temperature. After completion of the reaction, extraction was carried out by adding 1 M aqueous KHSO4 solution (100 mL) and dichloromethane (50 mL). The organic layer was separated, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure and co-evaporated with tetrahydrofuran (2×) to give 4.31 g (97% yield) of ethyl 1-(BOC-amino)cyclopropanecarboxylate.

[References]

[1] Patent: WO2015/90603, 2015, A1. Location in patent: Page/Page column 59; 60
[2] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 7, p. 2151 - 2155
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