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ChemicalBook--->CAS DataBase List--->60629-92-7

60629-92-7

60629-92-7 Structure

60629-92-7 Structure
IdentificationBack Directory
[Name]

1,1-DICYCLOPROPANECARBOXYLIC ACID
[CAS]

60629-92-7
[Synonyms]

1,1-Dicyclopanecarboxylic Acid
1,1-DICYCLOPROPANECARBOXYLIC ACID
-bi(cyclopropane)]-1-carboxylic acid
[1,1'-Bicyclopropyl]-1-carboxylic acid
1-cyclopropylcyclopropanecarboxylic acid
[1,1'-bi(cyclopropane)]-1-carboxylic acid
1-cyclopropylcyclopropane-1-carboxylic acid
[Molecular Formula]

C7H10O2
[MDL Number]

MFCD08704251
[MOL File]

60629-92-7.mol
[Molecular Weight]

126.15
Chemical PropertiesBack Directory
[Melting point ]

51-53℃
[Boiling point ]

239.9±8.0 °C(Predicted)
[density ]

1.389±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.78±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

1,1-DICYCLOPROPANECARBOXYLIC ACID(60629-92-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

benzyl 1-cyclopropylcyclopropane-1-carboxylate

1447944-40-2

1,1-DICYCLOPROPANECARBOXYLIC ACID

60629-92-7

General procedure for the synthesis of [1,1'-bicyclopropane]-1-carboxylic acid from the compound (CAS: 1447944-40-2): to a mixture of ester B-41a (100 mg, 0.462 mmol) dissolved in methanol (2.5 mL) and water (0.5 mL) at 0 °C was added an aqueous solution of 1 N NaOH (1 mL, 0.247 mmol ) and stirred at 0 °C for 10 min. The reaction mixture was then warmed to 25 °C and stirring was continued for 12 hours. After completion of the reaction, the volatile components were completely removed under reduced pressure. Water (5 mL) was added to the residue and extracted with ether (2 x 10 mL). The aqueous layer was adjusted to pH ~2 with 1.5 N HCl and then extracted with a 10% MeOH/DCM (3 × 10 mL) mixture. The organic layers were combined, washed with brine solution (10 mL) and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to afford [1,1'-bicyclopropane]-1-carboxylic acid (CapB-41) (60 mg, 0.476 mmol, 93% yield) as an off-white solid.1H NMR (CDCl3, δ=7.26 ppm, 400 MHz): δ1.49-1.46 (m, 1H), 1.15 (app. q J=3.6 Hz. 2H), 0.62 (app.q J=3.6 Hz, 2H), 0.49-0.44 (m, 2H), 0.04--0.008 (m, 2H).

[References]

[1] Patent: WO2015/5901, 2015, A1. Location in patent: Page/Page column 657; 658
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