تفاعل #46189

ord-6728d24891834364bf41775255c0d307

معادلة التفاعل

COC(=O)C1(c2ccc(OC)c(C(C)(C)O[SiH2]C(C)(C)C)c2)CC1
1-[3-(tert-butyl-dimethyl-silanyloxymethyl)-4-methoxy-phenyl]-cyclopropanecarboxylic acid methyl ester
O.[Li][OH]
LiOH.H2O
COc1ccc(C2(C(=O)O)CC2)cc1CO
1-(3-hydroxymethyl-4-methoxy-phenyl)-cyclopropanecarboxylic acid
المردود 132.5%

المذيبات

ظروف التفاعل

درجة الحرارة
40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىMeOH was removed by evaporation under vacuum
  2. 2
    workup.ADDITIONAcOH (1 mol/L, 40 mL) and EtOAc (200 mL) were added
  3. 3
    أخرىThe organic layer was separated
  4. 4
    غسيلwashed with brine
  5. 5
    تجفيفdried over anhydrous Na2SO4
  6. 6
    أخرىevaporated under vacuum

الإجراء التجريبي

To a solution of 1-[3-(tert-butyl-dimethyl-silanyloxymethyl)-4-methoxy-phenyl]-cyclopropanecarboxylic acid methyl ester (6.2 g, 18 mmol) in MeOH (75 mL) was added a solution of LiOH.H2O (1.50 g, 35.7 mmol) in water (10 mL) at 0° C. The reaction mixture was stirred overnight at 40° C. MeOH was removed by evaporation under vacuum. AcOH (1 mol/L, 40 mL) and EtOAc (200 mL) were added. The organic layer was separated, washed with brine, dried over anhydrous Na2SO4 and evaporated under vacuum to provide 1-(3-hydroxymethyl-4-methoxy-phenyl)-cyclopropanecarboxylic acid (5.3 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741321B2uspto-grants-2010_06