تفاعل #60772

ord-96c9846e5de44999b12d97648020fbad

معادلة التفاعل

N#CCc1ccc(Cl)c(Cl)c1
3,4-Dichloro-phenylacetonitrile
CC(Cl)Br
1-bromochoroethane
[Na+].[OH-]
sodium hydroxide
N#CC1(c2ccc(Cl)c(Cl)c2)CC1
title compound
المردود 102.4%
N#CC1(c2ccc(Cl)c(Cl)c2)CC1
1-(3,4-Dichloro-phenyl)-cyclopropanecarbonitrile
المردود 102.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise at 50°
  2. 2
    استخلاصextracted with EtOAc (×3)
  3. 3
    أخرىThe layers were separated
  4. 4
    غسيلwashed with water (×3) and brine
  5. 5
    تجفيفdried over MgSO4
  6. 6
    أخرىEvaporation of the solvent under reduced pressure

الإجراء التجريبي

To a stirred mixture of 3,4-Dichloro-phenylacetonitrile (4.65 g. 25 mmol) triethylbenzylammonium chloride (0.2 g) and 1-bromochoroethane (4.2 ml, 50 mmol), 50% sodium hydroxide (16 ml, 200 mmol) was added dropwise at 50° then the reaction was stirred at 50° for 10 hrs. After cooling to rt, the reaction mixture was diluted with water and extracted with EtOAc (×3). The layers were separated, washed with water (×3) and brine, then dried over MgSO4. Evaporation of the solvent under reduced pressure afforded the title compound (5.43 g) which was then recrystallized from Et2O/hexanes as a pale pink solid (4.49 g, 85%). Lc/MS(ES) m/e 212 [M+H]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07427623B2uspto-grants-2008_09