Pyridine → 4-(2'-Carboxy-2'-methylpropylmercapto)phenyl 2-phenylbutyrate

HRID 249538

반응식

HRID 249538 반응식
[C:1]1([CH:7]([CH2:11][CH3:12])[C:8](Cl)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:13][C:14]([CH3:27])([CH2:18][S:19][C:20]1[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][CH:21]=1)[C:15]([OH:17])=[O:16].N1C=CC=CC=1.CCOCC>C1COCC1>[C:1]1([CH:7]([CH2:11][CH3:12])[C:8]([O:26][C:23]2[CH:24]=[CH:25][C:20]([S:19][CH2:18][C:14]([C:15]([OH:17])=[O:16])([CH3:27])[CH3:13])=[CH:21][CH:22]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

6

실험 절차

A solution of 2-phenylbutyryl chloride (1.19 g, 6.5 mmol) in 5 mL of THF was added to a stirred solution of 2,2-dimethyl-3-(4'-hydroxyphenylthio)-propionic acid (1.36 g, 6.0 mmol) and pyridine (1.03 g, 13.0 mmol) in 10 mL of THF under N2. After 6 days, 30 mL of ether was added and the reaction mixture filtered into a separatory funnel. The organic layer was washed with 0.5N HCl (2×15 mL), saturated NaCl (15 mL), 1:9 saturated NaHCO3 /H2O (2×15 mL), saturated NaCl (15 mL) and dried over anhydrous MgSO4. Filtration and evaporation provided 1.96 g (88%) of the desired ester. 1H NMR (CDCl3) δ0.974 (t, 3H, J=7.2 Hz), 1.27 (s, 6H), 1.82-1.96 (m, 1H), 2.13-2.28 (m, 1H), 3.13 (s, 2H), 3.67 (t, 1H, J=7.5 Hz), 6.90 (d, 2H, J=8.7 Hz), 7.30-7.38 (ArH, 7H), 11.9 (br s, --OH); 13C NMR (CDCl3) δ11.84, 24.30, 26.45, 43.73, 44.95, 53.27, 122.06, 127.58, 128.01, 128.88, 131.66, 134.27, 138.58, 149.65, 172.75, 183.22.

후처리

  1. filtrationthe reaction mixture filtered into a separatory funnel
  2. washThe organic layer was washed with 0.5N HCl (2×15 mL), saturated NaCl (15 mL), 1:9 saturated NaHCO3 /H2O (2×15 mL), saturated NaCl (15 mL)
  3. dry with materialdried over anhydrous MgSO4
  4. filtrationFiltration and evaporation

출처 및 근거

ORD 기록
ord-98945d61aed44b88ab29dd8274c100ec
출처 데이터셋
uspto-grants-1993_05
특허 번호
US05214191

연결된 노트

불러오는 중…