تفاعل #9422

ord-919f5637e2fc42948973a9ffeda0599d

معادلة التفاعل

CCI
iodoethane
O=C1Cc2ccccc2N1
oxindole
[Li][CH2]CCC
n-butyl lithium
[Cl-].[NH4+]
NH4Cl
CN(C)CCN(C)C
N,N,N′,N′-tetramethylethylenediamine
CCC1=c2ccccc2=NC1=O
3-ethyl-indol-2-one
المردود 2.9%

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
  6. 6
    أخرىto afford the crude product (24.5 g, 51%)
  7. 7
    أخرىA sample (3 g) was recrystallized from EtOAc/hexane

الإجراء التجريبي

A solution of oxindole (40 g, 0.3 mol) in dry THF (400 ml) under N2 was cooled to −25° C. and treated drop wise with n-butyl lithium (2.5M in hexanes, 240 ml, 0.6 mol). To the resulting solution was added N,N,N′,N′-tetramethylethylenediamine (90.4 ml, 0.6 mol). After 30 min. iodoethane (48 ml, 0.6 mol) was added and the reaction mixture was allowed to warm to room temperature and stirred over night. The reaction mixture was poured into 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 the crude product (24.5 g, 51%). A sample (3 g) was recrystallized from EtOAc/hexane to obtain 3-ethyl-indol-2-one (1.4 g), m.p. 100–101° C.; 1H-NMR (DMSO-d6) δ 0.76 (t, 3H, J=7.5 Hz), 1.8–2.0 (m, 2H), 3.38 (t, 3H, J=5.7 Hz), 6.8 (dt, 1H, J=7.69, 0.45 Hz), 6.93 (dt, 1H, J=7.45, 1.10 Hz), 7.15 (m, 1H), 7.22 (m, 1H), 10.3 (s, 1H); MS (ESI) m/z 270 [M+H].

المصدر

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