تفاعل #330408

ord-1d39278d662249e5a56eb405fe82a9d0

معادلة التفاعل

CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
O=[N+]([O-])c1ccc(F)c(O)c1F
2,6-difluoro-3-nitrophenol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)(C)OC(=O)NCCCO
(3-hydroxypropyl)carbamic acid tert-butyl ester
CC(C)(C)OC(=O)NCCCOc1c(F)ccc([N+](=O)[O-])c1F
title compound
المردود 92.0%
CC(C)(C)OC(=O)NCCCOc1c(F)ccc([N+](=O)[O-])c1F
[3-(2,6-Difluoro-3-nitrophenoxy)propyl]carbamic acid tert-butyl ester
المردود 92.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was cooled in an ice bath
  2. 2
    تركيزconcentrated in vacuo
  3. 3
    أخرىThe resulting residue was purified by column chromatography (Si—PCC, eluant 25-40% EtOAc in cyclohexane)

الإجراء التجريبي

To a solution of 2,6-difluoro-3-nitrophenol (170 mg, 0.971 mmol) and triphenylphosphine (383 mg, 1.46 mmol) in THF (8 mL) was added a solution of (3-hydroxypropyl)carbamic acid tert-butyl ester (204 mg, 1.165 mmol) in THF (1 mL). The mixture was cooled in an ice bath and a solution of diethyl azodicarboxylate (255 mg, 1.46 mmol) in THF (1 mL) was added. The reaction was stirred at RT for 30 min, then concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, eluant 25-40% EtOAc in cyclohexane) affording the title compound as a colourless gum (296 mg, 92%). 1H NMR (CDCl3, 300 MHz): 7.81 (1H, ddd, J=9.4, 7.8, 5.3 Hz), 7.04 (1H, dt, J=9.4, 2.2 Hz), 4.77 (1H, bs), 4.27 (2H, t, J=6.0 Hz), 3.37 (2H, q, J=6.4 Hz), 2.00 (2H, quintet, J=6.3 Hz), 1.45 (9H, s)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08653089B2uspto-grants-2014_02