ChemicalBook--->CAS DataBase List--->10292-61-2

10292-61-2

10292-61-2 Structure

10292-61-2 Structure
IdentificationBack Directory
[Name]

4-CYCLOPROPYLPHENOL
[CAS]

10292-61-2
[Synonyms]

AKOS BAR-1183
4-CYCLOPROPYLPHENOL
4-Cyclopropylphenol98%
Phenol, p-cyclopropyl-
Phenol, 4-cyclopropyl-
4-Cyclopropylphenol 98%
(4-Hydroxyphenyl)cyclopropane
[Molecular Formula]

C9H10O
[MDL Number]

MFCD06802405
[MOL File]

10292-61-2.mol
[Molecular Weight]

134.18
Chemical PropertiesBack Directory
[Melting point ]

57-58℃
[Boiling point ]

248.2±19.0℃ (760 Torr)
[density ]

1.158±0.06 g/cm3 (20 ºC 760 Torr)
[refractive index ]

1.5618 (589.3 nm 20℃)
[Fp ]

119.8±11.0℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

10.05±0.13(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS05,GHS08,GHS09
[Signal word ]

Danger
[Hazard statements ]

H303-H314-H371-H373-H411
[Precautionary statements ]

P501-P273-P260-P270-P264-P280-P391-P308+P311-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405
[HS Code ]

2907199090
Spectrum DetailBack Directory
[Spectrum Detail]

4-CYCLOPROPYLPHENOL(10292-61-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Diiodomethane

75-11-6

4-Acetoxystyrene

2628-16-2

4-CYCLOPROPYLPHENOL

10292-61-2

To a solution of diethylzinc (59 mL, 65.9 mmol) in toluene (80 mL) was sequentially added 4-acetoxystyrene (5 mL, 32.7 mmol) and diiodomethane (6.86 mL, 85 mmol). The reaction mixture was stirred at room temperature for 5 hours and then heated to reflux for 12 hours. Upon completion of the reaction, the reaction was quenched with 2N HCl solution, the organic layer was separated, washed with brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to give a brown oily crude product (4.5 g). The crude product was dissolved in methanol/tetrahydrofuran (20 mL/20 mL) mixed solvent, sodium carbonate (5.41 g, 51.1 mmol) was added, and stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate and washed sequentially with saturated aqueous ammonium chloride solution and water, and the aqueous phase was back-extracted with ethyl acetate (3×). The organic phases were combined, dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford 4-cyclopropylphenol (3.2 g, 94% yield), the product could be used for subsequent reactions without further purification.

[References]

[1] Patent: US2011/105520, 2011, A1. Location in patent: Page/Page column 55
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