تفاعل #355764

ord-2e8442a9e4d74eb4a9187ceac3c4bb29

معادلة التفاعل

CN(C)C=O
DMF
CN(C)CCN(C)C
TMEDA
CC(C)(C)CCOc1cccc(OCCC(C)(C)C)c1
1,3-di(3,3-dimethylbutoxy)benzene
[Li][CH2]CCC
n-BuLi
CC(C)(C)CCOc1cccc(OCCC(C)(C)C)c1C=O
1,3-di(3,3-dimethylbutoxy)benzene
المردود 90.8%
CC(C)(C)CCOc1cccc(OCCC(C)(C)C)c1C=O
2,6-Bis(3,3-dimethylbutoxy)benzaldehyde
المردود 90.8%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas warmed to room temperature
  2. 2
    workup.STIRRINGafter 2 h of stirring
  3. 3
    أخرىthe reaction was quenched with water
  4. 4
    استخلاصextracted with ether (4×300 mL)
  5. 5
    أخرىseparated
  6. 6
    أخرىevaporated
  7. 7
    أخرىThe product was purified by chromatography on silica using 9:1 hexanes

الإجراء التجريبي

TMEDA (23.0 g, 0.198 mol), 1,3-di(3,3-dimethylbutoxy)benzene (46.2 g, 0.166 mol) and ether (500 mL) were brought together in a two-neck 1-L flask fitted with a nitrogen inlet and a pressure-equalizing addition funnel. The reaction mixture was cooled to 0° C., and deaerated. n-BuLi (2.5 M solution in hexanes, 0.18 mol) was added dropwise over a period of 30 min via the addition funnel. The mixture was stirred for 3 h, following which that time it was warmed to room temperature. At this point DMF (23.0 g, 0.315 mol) was added dropwise; after 2 h of stirring, the reaction was quenched with water, extracted with ether (4×300 mL), separated, and evaporated. The product was purified by chromatography on silica using 9:1 hexanes:ethyl acetate as the eluant, giving 36.6 g of product (72% yield, based on 46.2 g of the 1,3-di(3,3-dimethylbutoxy)benzene starting material). 1H NMR (250 MHz, CDCl3): 10.49 (s, 1H), 7.37 (t, 1H, J=8.5 Hz), 6.52 (d, 2H, J=8.5 Hz), 4.06 (t, 4H, J=7.2 Hz), 1.76 (t, 4H, J=7.2 Hz), 0.96 (s, 18H). HRMS (ESI+) m/z: 329.2107 (calcd for C19H30O3Na (M+Na)+ 329.2092).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07445845B2uspto-grants-2008_11