تفاعل #685019

ord-4d3dafde7f144866bfe196a2dd1a3621

معادلة التفاعل

O=C1CCN(C(=O)OCc2ccccc2)C1
benzyl 3-oxopyrrolidine-1-carboxylate
OCCO
ethylene glycol
O=C(OCc1ccccc1)N1CCC2(C1)OCCO2
desired product
المردود 101.4%
O=C(OCc1ccccc1)N1CCC2(C1)OCCO2
Benzyl 1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxylate
المردود 101.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux
  2. 2
    درجة الحرارةthe reaction mixture was cooled
  3. 3
    غسيلwashed with water (2×25 mL), brine (25 mL)
  4. 4
    تجفيفdried (MgSO4)
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated
  7. 7
    أخرىto give yellow oil
  8. 8
    أخرىFlash column chromatography purification on silica gel column with 1:4

الإجراء التجريبي

A solution of benzyl 3-oxopyrrolidine-1-carboxylate (11.2 g, 51.09 mmol), ethylene glycol (2.4 g, 38.67 mmol) and TsOH.H2O (10 mg) in benzene (100 mL) was heated at reflux using Dean-Stork condenser. After 20 h, the reaction mixture was cooled, diluted with EtOAc (100 mL), washed with water (2×25 mL), brine (25 mL), dried (MgSO4), filtered and concentrated to give yellow oil. Flash column chromatography purification on silica gel column with 1:4 followed by 3:7 EtOAc:hexanes provided desired product (10.32 g, 100%) as colorless liquid. 1H NMR (500 MHz, CDCl3) δ: 7.38-7.28 (5H, m), 5.13 (2H, s), 3.99-3.92 (4H, m), 3.58-3.54 (2H, m), 3.45 (2H, d, J=10.7 Hz), 2.07-2.02 (2H, m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897593B2uspto-grants-2011_03