تفاعل #9423

ord-2b44cd7d278c4cc8bad2b58a6a049672

معادلة التفاعل

CCI
iodoethane
CCC1=c2ccccc2=NC1=O
3-ethyl-indol-2-one
[Li][CH2]CCC
n-butyllithium
[Cl-].[NH4+]
NH4Cl
CN(C)CCN(C)C
N,N,N′,N′-tetramethylethylenediamine
CCC1(CC)C(=O)Nc2ccccc21
3,3-diethylindol-2-one
المردود 47.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with EtOAc (2×)
  2. 2
    غسيلthe combined organic layers were washed with dil. HCl, water, brine
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe residual oil was triturated with hexane

الإجراء التجريبي

A solution of 3-ethyl-indol-2-one (16 g, 0.1 mol) in dry THF (200 ml) under N2 was cooled to −25° C. and treated drop wise with n-butyllithium (2.5M in hexanes, 80 ml, 0.2 mol). To the resulting solution was added N,N,N′,N′-tetramethylethylenediamine (30 ml, 0.2 mol). After 30 min. iodoethane (8 ml, 0.1 mol) was added and the reaction mixture was allowed to warm to RT and stirred over night. The reaction mixture was poured into an aqueous NH4Cl solution, extracted with EtOAc (2×) and the combined organic layers were washed with dil. HCl, water, brine, dried (MgSO4) and concentrated. The residual oil was triturated with hexane to afford 3,3-diethylindol-2-one (9 g, 45%), m.p. 156–159° C.; 1H NMR (DMSO-d6) δ 10.44 (s, 1H), 7.70–7.69 (t, 1H), 7.62–7.59 (m, 1H), 7.58 (d, 1H J=1.7 Hz), 7.53–7.50 (m, 1H), 7.45–7.41 (t, 1H), 7.36–7.35 (m, 1H), 7.34–7.33 (m, 1H), 6.91–6.89 (d, 1H J=8.2 Hz), 1.87–1.80 (m, 2H), 1.77–1.70 (m, 2H), 0.54–0.50 (t, 6H); MS/ (+ESI) m/z 190 (M+H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091234B2uspto-grants-2006_08