반응 #1178417

ord-09c748aa03c44f4fbd12e6af789a1809

반응 방정식

NC1(C(=O)O)CC1
1-aminocyclopropanecarboxylic acid
COc1cccc(C(=O)Cl)c1C
3-methoxy-2-methylbenzoyl chloride
COc1cccc(C2=NC3(CC3)C(=O)O2)c1C
5-(3-methoxy-2-methyl-phenyl)-6-oxa-4-aza-spiro[2.4]hept-4-en-7-one
수율 78.3%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타evaporated under reduced pressure
  2. 2
    기타to leave an oily solid
  3. 3
    세척washed with water (50 mL), 5% aqueous HCl (2×50 mL) and saturated aqueous NaHCO3 (50 mL)
  4. 4
    건조The organic layer was dried over MgSO4
  5. 5
    기타evaporated under reduced pressure

실험 절차

To a stirred solution of 1-aminocyclopropanecarboxylic acid (1.06 g, 10.5 mmol) in pyridine (20 mL) cooled to ˜5° C., solid 3-methoxy-2-methylbenzoyl chloride (4.35 g, 23.6 mmol) was added. The mixture was stirred at room temperature for 1 week and evaporated under reduced pressure to leave an oily solid. This material was taken up in 20% ether in hexanes (175 mL), washed with water (50 mL), 5% aqueous HCl (2×50 mL) and saturated aqueous NaHCO3 (50 mL). The organic layer was dried over MgSO4 and evaporated under reduced pressure to leave 5-(3-methoxy-2-methyl-phenyl)-6-oxa-4-aza-spiro[2.4]hept-4-en-7-one (1.90 g) as a yellow solid. 1H NMR (CDCl3) δ (ppm): 1.80 (m, 2H), 1.90 (m, 2H), 2.49 (s, 3H), 3.85 (s, 3H), 7.01 (d, 1H), 7.22 (t, 1H), 7.40 (d, 1H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08129355B2uspto-grants-2012_03