تفاعل #9063

ord-9063122c42f54bc49e4e673ee2153a6a

معادلة التفاعل

COC(=O)c1ccc(-c2nc3ccccc3[nH]2)cc1
methyl 4-(benzimidazol-2-yl)-benzoate
CC(C)[CH2][AlH][CH2]C(C)C
DIBAL-H
OCc1ccc(-c2nc3ccccc3[nH]2)cc1
4-(benzimidazol-2-yl)-benzyl alcohol
المردود 87.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with a saturated potassium sodium tartrate solution (20 mL)
  2. 2
    workup.STIRRINGThe biphasic mixture was stirred vigorously for 1 h
  3. 3
    أخرىthe phases separated
  4. 4
    تجفيفthe organic layer dried (MgSO4)
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated
  7. 7
    أخرىpurified by column chromatography on silica gel (7% MeOH/CH2Cl2)

الإجراء التجريبي

To a solution of methyl 4-(benzimidazol-2-yl)-benzoate (0.23 g, 0.9 mmol) in THF (10 mL) at 0° C. was added a solution of DIBAL-H (5.0 mL, 1.0 M in THF, 5.0 mmol). The reaction was allowed to warm to room temperature, stirred for 1 h and quenched with a saturated potassium sodium tartrate solution (20 mL). The biphasic mixture was stirred vigorously for 1 h, the phases separated and the organic layer dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (7% MeOH/CH2Cl2) to give 4-(benzimidazol-2-yl)-benzyl alcohol (0.175 g, 87%). 1H NMR (CD4OD) δ 3.30 (s, 1H (OH)), 4.69 (s, 2H), 7.26 (m, 2H), 7.53 (d, 2H, J=8.4 Hz), 7.60 (m, 2H), 8.07 (d, 2H, J=8.1 Hz).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091217B2uspto-grants-2006_08