Sulfuric Acid → Benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid

HRID 2222982

반응식

HRID 2222982 반응식
[CH2:1]([O:8][C:9]([NH:11][CH:12](O)[C:13]([OH:15])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[O:24][CH3:25].S(=O)(=O)(O)O>C(O)(=O)C>[CH2:1]([O:8][C:9]([NH:11][CH:12]([C:22]1[CH:21]=[CH:20][C:19]([O:24][CH3:25])=[C:18]([CH3:17])[CH:23]=1)[C:13]([OH:15])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 336372-MethylanisoleHCID 35095062-(((Benzyloxy)carbonyl)amino)-2-hydroxyacetic acid

생성물 1

HCID 68798586Benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid수율 100%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of benzyloxycarbonylamino-hydroxy-acetic acid (5.9 g, 26.2 mmol) (prepared according to the procedure of E. H. W. Bohme, et al., J. Med. Chem, 1980, 23, 405-412) and 2-methylanisole (3.2 g, 26.2 mmol) in acetic acid (150 mL) was added concentrated sulfuric acid (15 mL). The mixture was stirred at room temperature for 1 hour, then poured into ice/water and extracted with ethyl acetate (2×200 mL). The combined organic extracts were dried over sodium sulfate and concentrated to give an oily residue. The residue was triturated in hexanes, the precipitate formed was collected by filtration and dried overnight to give crude benzyloxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid as a white solid (8.6 g, 100%).

후처리

  1. extractionextracted with ethyl acetate (2×200 mL)
  2. dry with materialThe combined organic extracts were dried over sodium sulfate
  3. concentrationconcentrated
  4. customto give an oily residue
  5. customThe residue was triturated in hexanes
  6. customthe precipitate formed
  7. filtrationwas collected by filtration
  8. customdried overnight

출처 및 근거

ORD 기록
ord-789344fc26cb45b19583704352d755b1
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07371869B2

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