تفاعل #2200626

ord-6530221df8e146b88a595c730cc7a3c8

معادلة التفاعل

O=C=O
dry ice
[Li][C](C)(C)C
Tert.-butyllithium
Fc1ccc(OC(F)(F)F)cc1
1-fluoro-4-trifluoromethoxy-benzene
CN(C)C=O
DMF
O=Cc1cc(OC(F)(F)F)ccc1F
title compound
المردود 53.0%
O=Cc1cc(OC(F)(F)F)ccc1F
2-Fluoro-5-trifluoromethoxy-benzaldehyde
المردود 53.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas kept <−70° C
  2. 2
    أخرىtemperature <−70° C
  3. 3
    workup.WAITAfter 30 min the reaction mixture was allowed
  4. 4
    أخرىto reach rt
  5. 5
    أخرىquenched with saturated NH4Cl solution
  6. 6
    استخلاصextracted with ether
  7. 7
    غسيلThe organic phase was washed with brine
  8. 8
    تركيزconcentrated
  9. 9
    أخرىchromatographed (SiO2, heptane:ethyl acetate=100:0 to 80:2)

الإجراء التجريبي

A solution of 1-fluoro-4-trifluoromethoxy-benzene (21.0 g, 117 mmol) in THF (233 ml) was cooled to <−70° C. Tert.-butyllithium (86 ml of a 1.5 molar solution in pentane, 129 mmol) was added at such a rate that temperature was kept <−70° C. Stirring in the dry ice bath was continued for 15 min, then DMF (11.6 ml, 150 mmol) was added dropwise keeping temperature <−70° C. After 30 min the reaction mixture was allowed to reach rt, quenched with saturated NH4Cl solution and extracted with ether. The organic phase was washed with brine, concentrated and chromatographed (SiO2, heptane:ethyl acetate=100:0 to 80:2). The title compound (11.0 g, 53%) was obtained as a light yellow oil. 1H-NMR (300 MHz, DMSO): δ=7.60 (t, J=9.2 Hz, 1H), 7.75-7.85 (m, 2H), 10.20 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07432256B2uspto-grants-2008_10