تفاعل #478763

ord-af2d4656b72d40e48d9ac3811dfd53e8

معادلة التفاعل

NC(=O)C(F)(F)F
trifluoroacetamide
COC(=O)CCc1ccc(S(C)=O)cc1
methyl 3-(4-(methylsulfinyl)phenyl)propanoate
COC(=O)CCc1ccc(S(C)(=O)=NC(=O)C(F)(F)F)cc1
title compound
المردود 69.0%
COC(=O)CCc1ccc(S(C)(=O)=NC(=O)C(F)(F)F)cc1
Methyl 3-{4-[S-methyl-N-(trifluoroacetyl)sulfonimidoyl]phenyl}-propanoate
المردود 69.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthen filtered through celite
  2. 2
    أخرىThe resulting residue was purified via column chromatography (silica gel, gradient eluant mixture: 20% EtOAc in hexanes to 100% EtOAc)

الإجراء التجريبي

In a 100 mL round bottom flask, methyl 3-(4-(methylsulfinyl)phenyl)propanoate (0.4 g, 1.77 mmol) was added to CH2Cl2 (18 mL). Subsequently the reaction was treated with MgO (0.285 g, 7.08 mmol), trifluoroacetamide (0.400 g, 3.54 mmol), PhI(OAc)4 (0.884 g, 2.66 mmol), and Rh2(OAc)4 (19.55 mg, 0.0443 mmol). The suspension was stirred overnight then filtered through celite. The filtrate was the concentrated. The resulting residue was purified via column chromatography (silica gel, gradient eluant mixture: 20% EtOAc in hexanes to 100% EtOAc) to give the title compound (0.294 g, 69%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08383825B2uspto-grants-2013_02