تفاعل #85593

ord-4d827cc537484e228c849fdeaddc49cf

معادلة التفاعل

Cc1cc(O)ccc1[N+](=O)[O-]
3-methyl-4-nitrophenol
FC(F)(F)COCC(F)(F)F
trifluoroethyl ether
[O-]c1ccccc1
phenolate
Cc1ccc(S(=O)(=O)OCC(F)(F)F)cc1
2,2,2-trifluoroethyl tosylate
c1ccc2[nH]ccc2c1
indole
[H-].[Na+]
sodium hydride
O=C(O)c1c[nH]c2ccc(OCC(F)(F)F)cc12
title compound
O=C(O)c1c[nH]c2ccc(OCC(F)(F)F)cc12
5-(2,2,2-trifluoroethoxy)-1H-indole-3-carboxylic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرى5-(2,2,2-trifluoroethoxy)-1H-indole-3-carboxylic acid was prepared
  2. 2
    أخرىreported in Synthesis (1980) 727

الإجراء التجريبي

5-(2,2,2-trifluoroethoxy)-1H-indole-3-carboxylic acid was prepared following the procedure reported in Synthesis (1980) 727. 3-methyl-4-nitrophenol (Aldrich) was deprotonated with sodium hydride in HMPA, and the resulting phenolate alkylated with 2,2,2-trifluoroethyl tosylate (Aldrich). The resulting trifluoroethyl ether was then converted to the indole using the Batcho-Leimgruber protocol. Formylation and oxidation as described herein gave the title compound as an off-white solid. MS (m/e) 260.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09434724B2uspto-grants-2016_09