반응 #66050

반응 방정식

96

Methyl (2S)-2-acetamido-3-(4-[9-anthracenyl]phenyl)-propanoate

lithium hydroxide monohydrate

→

title compound

수율 90.0%

(2S)-2-Acetamido-3-(4-[9-anthracenyl]phenyl) propanoic acid

수율 90.0%

용매

water

THF water

반응 조건

후처리

1. 1
   기타the THF was removed by evaporation
2. 2
   세척The aqueous layer was washed with DCM (40 mL)
3. 3
   기타to remove unreacted
4. 4
   추출the resulting precipitate was extracted with DCM (3×40 mL)
5. 5
   기타The combined organics were dried
6. 6
   기타evaporated

실험 절차

To a solution of 96 (80 mg, 0.20 mmol) in THF/water, 2:1 (3 mL) was added lithium hydroxide monohydrate (17 mg, 0.40 mmol) and the resulting suspension was allowed to stir for 16 h. The reaction mixture was diluted with water (30 mL) and the THF was removed by evaporation. The aqueous layer was washed with DCM (40 mL) to remove unreacted starting material. The aqueous phase was acidified with 10% HCl and the resulting precipitate was extracted with DCM (3×40 mL). The combined organics were dried and evaporated to yield the title compound (69 mg, 0.18 mmol, 90%) as a white solid. Mp 76° C. [α]D20 +29.7 (c. 0.1, EtOH). 1H NMR (CDCl3, 300 MHz): δ 8.47 (s, 1H, ArH10″); 8.02 (d, J=8.4 Hz, 2H, ArH3″ and ArH6″); 7.59 (d, J=8.7 Hz, 2H, ArH8″ and ArH1″); 7.45 (m, 2H, ArH4″ and ArH5″); 7.35 (m, 6H, ArH2″ and ArH7″, 4×ArH″); 6.27 (d, J=6.6 Hz, 1H, NH); 5.00 (m, 1H, H2); 3.39 (dd, J=4.8, 12.9 Hz, 1H, H3a); 3.26 (dd, J=6.3, 14.4 Hz, 1H, H3b); 2.07 (s, 3H, COCH3). Mass Spectrum (ES, +ve) m/z 383 (70%) [MH+]. HRMS calcd for C25H22NO3 384.1600, found 384.1610.

출처