تفاعل #2310220

ord-59f1303ed5e947228fc2b2ee935b28b3

معادلة التفاعل

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-oxa4-aza-spiro[2.4]hept-4-en-7-one
المردود 78.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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-oxa4-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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07375093B2uspto-grants-2008_05