반응 #8432

ord-8008fa54facc4b4e9dcdeff3d5d00384

반응 방정식

O=S(=O)([O-])[O-].[Mg+2]
MgSO4
[H-].[Na+]
NaH
Brc1ccc2[nH]ccc2c1
5-Bromoindole
CC(C)[Si](Cl)(C(C)C)C(C)C
triisopropylsilyl chloride
CC(C)[Si](C(C)C)(C(C)C)n1ccc2cc(Br)ccc21
5-Bromo-1-triisopropylsilyl-indole
수율 85.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter 3 h
  2. 2
    여과The mixture was filtered
  3. 3
    농축concentrated
  4. 4
    기타The product was obtained as a pale yellow oil (5.96 g, 17 mmol; yield 85%)

실험 절차

5-Bromoindole (3.92 g; 20 mmol) was dissolved in DCM (100 mL) and DMF (1 mL). NaH (0.88 g, 22 mmol; 60% in oil) was added to the cooled solution. After stirring for 15 minutes, triisopropylsilyl chloride (3.86 g, 20 mmol) was added dropwise to the reaction mixture. After 3 h, water (1 mL) was added, followed by MgSO4. The mixture was filtered and concentrated and the residue put through a silica column with hexane as eluent. The product was obtained as a pale yellow oil (5.96 g, 17 mmol; yield 85%). 1H NMR (CDCl3) δ 1.13 (18 H, d, J=8), 1.67 (3 H, m), 6.55 (1 H, d, J=3), 7.21 (1 H, dd, J=9, 2), 7.24 (1 H, d, J=3), 7.36 (1 H, d, J=9) and 7.74 (1 H, d, J=2).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087750B2uspto-grants-2006_08