تفاعل #7058

ord-4011bed5f5294dad8742b47fef93d11e

معادلة التفاعل

COc1cc(S(N)(=O)=O)sc1[Si](C)(C)C
5-trimethylsilyl-4-methoxythiophene-2-sulfonamide
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
tetra-butylammonium fluoride
COc1csc(S(N)(=O)=O)c1
title compound
المردود 86.0%
COc1csc(S(N)(=O)=O)c1
4-Methoxythiophene-2-sulfonamide
المردود 86.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe THF is removed under reduced pressure
  2. 2
    workup.DISSOLUTIONThe residue is dissolved in EtOAc (200 mL)
  3. 3
    غسيلThe organic layer is washed with brine
  4. 4
    تجفيفthen dried (Na2SO4)
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe crude product is chromatographed on silica gel
  8. 8
    غسيلeluting with Hex

الإجراء التجريبي

To a solution of 5-trimethylsilyl-4-methoxythiophene-2-sulfonamide (770 mg, 2.90 mmol) in THF (10 mL) is added a solution of tetra-butylammonium fluoride (17.4 mL of 1 M in THF, 17.4 mmol). The reaction mixture is stirred at room temperature for 2 hr. The THF is removed under reduced pressure. The residue is dissolved in EtOAc (200 mL). The organic layer is washed with brine then dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with Hex:EtOAc (3:1) to afford the title compound (480 mg, 86%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084170B2uspto-grants-2006_08