تفاعل #439270

ord-1711970a47774366af95222e22a27154

معادلة التفاعل

C=COCC1CCC(CO)CC1
4-cyclohexanedimethanol vinyl ether
CC#N
acetonitrile
FC(F)=C(F)Cl
chlorotrifluoroethylene
C=COCC1CCC(COC(F)(F)C(C)(F)Cl)CC1
desired product
المردود 58.0%
C=COCC1CCC(COC(F)(F)C(C)(F)Cl)CC1
2-Chloro-1,1,2-trifluoro-1-{[4-(vinyloxymethyl)cyclohexyl]methoxy}propane
المردود 58.0%

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىpartially evacuated
  2. 2
    أخرىcondensed
  3. 3
    درجة الحرارةAfter this, the PARR® reactor was cooled to room temperature
  4. 4
    أخرىseparated
  5. 5
    تركيزwas concentrated under reduced pressure 0.05 mmHg) at 25-30° C.

الإجراء التجريبي

Into a 450 mL capacity PARR® reactor, 1,.4-cyclohexanedimethanol vinyl ether (50 g, 294 mmol), acetonitrile (100 mL), and Cs2CO3 (2 g, 6 mmol) were added. The PARR® reactor was cooled to ˜30° C., partially evacuated and chlorotrifluoroethylene (34 g, 294 mmol) was condensed and the resultant mixture was heated at ˜50-60° C with stirring for 3 hours. After this, the PARR® reactor was cooled to room temperature, vented in the fume hood and the reaction mixture was poured into ˜150 mL water and the lower layer containing the crude product separated, and was concentrated under reduced pressure 0.05 mmHg) at 25-30° C. to afford the desired product as a colorless viscous liquid (49 g, 58% yield) which is a mixture of cis/trans isomers in the ratio 73:18; refractive index of 1.415 at 23.7° C.; GC/MS (EI mode): m/z at 286 for M+; 19F and 1H NMR spectral data are consistent with the structure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06743943B2uspto-grants-2004_06