تفاعل #155409

ord-88e9b5916c4b4a1eaa9fc78604d5ac0e

معادلة التفاعل

O=C([O-])[O-].[K+].[K+]
potassium carbonate
BrCc1ccccc1
Benzyl bromide
O=Cc1ccc(B(O)O)cc1
4-formylbenzeneboronic acid
O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
O=Cc1ccc(Cc2ccccc2)cc1
title compound
المردود 83.0%
O=Cc1ccc(Cc2ccccc2)cc1
4-Benzylbenzaldehyde
المردود 83.0%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool to ambient temperature
  2. 2
    استخلاصextracted with ethyl acetate (3-fold 50 mL)
  3. 3
    غسيلThe combined organic extracts were washed with brine (100 mL)
  4. 4
    تجفيفdried (magnesium sulphate)
  5. 5
    أخرىthe solvent removed in vacuo
  6. 6
    أخرىThe resulting oil was purified by column chromatography on silica gel eluting with ethyl acetate

الإجراء التجريبي

Benzyl bromide (41 g, 240 mmol), 4-formylbenzeneboronic acid (28 g, 186.7 mmol), palladium tetrakis triphenyl phosphine (7.9 g, 6.84 mmol) and potassium carbonate (84.7 g, 613 mmol) were combined in tetrahydrofuran (620 mL) and heated at 80° C. under nitrogen for 8 hours. The resulting suspension was allowed to cool to ambient temperature and stirred overnight. The reaction mixture was poured into 10% citric acid (50 mL) and extracted with ethyl acetate (3-fold 50 mL). The combined organic extracts were washed with brine (100 mL) and dried (magnesium sulphate) and the solvent removed in vacuo. The resulting oil was purified by column chromatography on silica gel eluting with ethyl acetate:heptane, (0:1 changing to 1:5, by volume) to give the title compound as a colourless oil, 83% yield, 30.45 g.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08822439B2uspto-grants-2014_09