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ChemicalBook CAS DataBase List ethyl 2-(4,4-difluorocyclohexyl)acetate
915213-54-6

ethyl 2-(4,4-difluorocyclohexyl)acetate synthesis

3synthesis methods
ethyl 4-oxocyclohexaneacetate

58012-34-3

ethyl 2-(4,4-difluorocyclohexyl)acetate

915213-54-6

General steps: 1. ethyl 2-(4-oxocyclohexyl)acetate (0.4 g) was dissolved in dichloromethane (DCM, 5 mL) and Deoxo-Fluor (0.881 mL) and ethanol (EtOH, 0.038 mL) were added. 2. The reaction mixture was stirred at room temperature for 16 hours. 3. Upon completion of the reaction, the reaction mixture was diluted with saturated sodium bicarbonate (NaHCO3) solution and extracted with ethyl acetate (EtOAc). 4. The organic phase was separated, washed with water and then with saturated sodium chloride (NaCl) solution. 5. The organic phase was dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated to give ethyl 2-(4,4-difluorocyclohexyl)acetate (0.4 g). 6. 2-(4,4-difluorocyclohexyl)ethyl acetate was dissolved in tetrahydrofuran (THF, 2 mL) and 1N sodium hydroxide (NaOH, 1 mL) solution was added. 7. The reaction mixture was stirred at room temperature for 16 hours. 8. Upon completion of the reaction, the reaction mixture was concentrated and then diluted with ethyl acetate (EtOAc) and acidified with 1N hydrochloric acid (HCl). 9. The organic phase was washed with saturated aqueous sodium bicarbonate (NaHCO3) solution and then with saturated sodium chloride (NaCl) solution. 10. The organic phase was dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated to give 2-(4,4-difluorocyclohexyl)acetic acid as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 12.13 (1H, br.s.), 2.06-2.28 (3H, m), 1.92-2.03 (1H, m), 1.72-1.91 (4H, m), 1.31-1.48 (1H, m), 1.10-1.31 (2H, m).

1283719-20-9 Synthesis
Acetic acid, 2-(4,4-difluorocyclohexylidene)-, ethyl ester

1283719-20-9
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Yield:915213-54-6 98%

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in methanol at 20; under 750.075 Torr; for 16 h;

References:

Bamborough, Paul;Chung, Chun-Wa;Furze, Rebecca C.;Grandi, Paola;Michon, Anne-Marie;Watson, Robert J.;Mitchell, Darren J.;Barnett, Heather;Prinjha, Rab K.;Rau, Christina;Sheppard, Robert J.;Werner, Thilo;Demont, Emmanuel H. [Journal of Medicinal Chemistry,2018,vol. 61,# 18,p. 8321 - 8336]

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