تفاعل #161000

ord-d2bb77af91dd4b7eae884941754e58c0

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
CCOC(C)=O
ethyl acetate
NC1(C(=O)O)CCCCC1
1-aminocyclohexanecarboxylic acid
[Na+].[OH-]
sodium hydroxide
O=C(Cl)c1ccco1
2-furancarbonyl chloride
O=C(NC1(C(=O)O)CCCCC1)c1ccco1
title compound
O=C(NC1(C(=O)O)CCCCC1)c1ccco1
1-[(2-Furanylcarbonyl)amino]cyclohexanecarboxylic acid

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITover approximately 1 hour
  2. 2
    أخرىwas slowly returned to room temperature
  3. 3
    workup.STIRRINGstirred overnight
  4. 4
    workup.STIRRINGthe mixture was stirred for 1 hour
  5. 5
    أخرىthe insolubles were removed by filtration
  6. 6
    أخرىThe aqueous layer was separately collected
  7. 7
    workup.ADDITION49 ml of concentrated hydrochloric acid was added
  8. 8
    درجة الحرارةunder ice-cooling
  9. 9
    ترشيحThe precipitated crystal was collected by filtration and dried-under reduced pressure

الإجراء التجريبي

71.6 g (0.5 mol) of 1-aminocyclohexanecarboxylic acid was added to a solution of 20 g (0.5 mol) of sodium hydroxide in 250 ml of water, and the mixture was stirred at 80° C. for 2 hours. The mixture solution was cooled by ice-water, 71.8 g (0.2 mol) of 2-furancarbonyl chloride and a solution of 24 g (0.6 mol) of sodium hydroxide in 100 ml of water were simultaneously added thereto over approximately 1 hour. The reaction solution was slowly returned to room temperature and stirred overnight. After 80 ml of ethyl acetate was added to the reaction solution and the mixture was stirred for 1 hour, the insolubles were removed by filtration. The aqueous layer was separately collected, 49 ml of concentrated hydrochloric acid was added thereto under ice-cooling. The precipitated crystal was collected by filtration and dried-under reduced pressure to obtain 112.6 g (95%) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08829209B2uspto-grants-2014_09