反応 #706823

反応方程式

ethyl 4-[[4-(4-methylphenyl)-2,2-dimethyl-(2H)-thiochromen-6-yl]-ethynyl]-2-fluorobenzoate

Compound 236

ethyl 4-[[4-(4-methylphenyl)-2,2-dimethyl-(2H)-thiochromen-6-yl]-ethynyl]-2-fluorobenzoate

NaOH

HCl

→

title compound

収率 83.1%

4-[[4-(4-methylphenyl)-2,2-dimethyl-(2H)-thiochromen-6-yl]-ethynyl]-2-fluorobenzoic acid

収率 83.1%

溶媒

THF

EtOH

反応条件

後処理

1. 1
   温度Upon cooling to room temperature the reaction mixture
2. 2
   抽出extracted with EtOAc
3. 3
   洗浄The combined organic layers were washed with H2O, saturated aqueous NaCl
4. 4
   乾燥dried (Na2SO4)
5. 5
   その他before removing the solvent under reduced pressure
6. 6
   その他The residual solid was recrystallized from CH3CN

実験手順

To a solution of ethyl 4-[[4-(4-methylphenyl)-2,2-dimethyl-(2H)-thiochromen-6-yl]-ethynyl]-2-fluorobenzoate (Compound 236, 100.0 mg, 0.219 mmol) in 3.0 mL THF and 3.0 mL EtOH was added NaOH (80.0 mg, 2.0 mmol, 2.0 mL of a 1M aqueous solution). The resulting solution was heated to 40° C. and stirred overnight. Upon cooling to room temperature the reaction mixture was acidified with 10% aqueous HCl and extracted with EtOAc. The combined organic layers were washed with H2O, saturated aqueous NaCl, and dried (Na2SO4) before removing the solvent under reduced pressure. The residual solid was recrystallized from CH3CN to give 78.0 mg (83%) of the title compound as a pale-yellow solid. 1H NMR (300 MHz, d6 -acetone) δ: 7.94 (1H, d, J=7.8 Hz), 7.43-7.17 (9H, m), 5.93 (1H, s), 2.38 (3H, s), 1.47 (6H, s).

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