تفاعل #1909782

ord-b78871c01c914e5bac1d3403fdd3161f

معادلة التفاعل

O
Water
CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CC1
1-tert-butoxycarbonylisonipecotic acid ethyl ester
CC(C)[N-]C(C)C.[Li+]
lithium diisopropyl-amide
CCI
Ethyl iodide
CCOC(=O)C1(CC)CCN(C(=O)OC(C)(C)C)CC1
title compound
المردود 92.0%
CCOC(=O)C1(CC)CCN(C(=O)OC(C)(C)C)CC1
1-tert-Butoxycarbonyl-4-ethylisonipecotic acid ethyl ester
المردود 92.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred for 18 hours
  2. 2
    استخلاصthe mixture was extracted with ethyl acetate
  3. 3
    غسيلThe organic layer was washed successively with 1N hydrochloric acid, water and saturated brine
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    تركيزThe organic layer was concentrated under reduced pressure

الإجراء التجريبي

To a solution of 1-tert-butoxycarbonylisonipecotic acid ethyl ester (576 mg) in THF (15 ml) was added a solution of lithium diisopropyl-amide (290 mg) in THF (10 ml) in a stream of argon gas at −78° C., and the reaction mixture was stirred at the same temperature for 1 hour. Ethyl iodide (0.36 ml) was added to the above solution at −78° C., and the mixture was stirred for 18 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with 1N hydrochloric acid, water and saturated brine, and dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure to give the title compound (585 mg, yield 92%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE039088E1uspto-grants-2006_05