تفاعل #57507

ord-d0ee29176b5a419dbe118db7484bbd5e

معادلة التفاعل

[Na+].[OH-]
NaOH
CC(C)N(C(=O)CC(O)c1ccccc1)C(C)C
N,N-diisopropyl-3-phenyl-3-hydroxy-propionamide
Cc1ccc(O)cc1
p-cresol
Cc1ccc(O)c(C(CC(=O)N(C(C)C)C(C)C)c2ccccc2)c1
product
المردود 34.5%
Cc1ccc(O)c(C(CC(=O)N(C(C)C)C(C)C)c2ccccc2)c1
3-(2-hydroxy-5-methyl-phenyl)-N,N-diisopropyl-3-phenyl-propionamide
المردود 34.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA three-necked round-bottom flask equipped with condenser, mechanical stirrer
  2. 2
    workup.WAITleft
  3. 3
    workup.STIRRINGunder stirring for 30 minutes
  4. 4
    أخرىThe phases are separated
  5. 5
    استخلاصthe aqueous phase is extracted with toluene (2×30 ml)
  6. 6
    تجفيفThe combined organic phases are dried over sodium sulfate
  7. 7
    أخرىevaporated to dryness
  8. 8
    أخرىThe resulting oil is purified by flash chromatography (hexane/ethyl acetate 7:3)

الإجراء التجريبي

A three-necked round-bottom flask equipped with condenser, mechanical stirrer, thermometer, is loaded with N,N-diisopropyl-3-phenyl-3-hydroxy-propionamide (1.0 g; 0.0041 mol), p-cresol (0.48 g; 0.0044 mol) and polyphosphoric acid (16.5 g). After five hours under stirring at room temperature the reaction is completed. The reaction mixture is poured in ice/water (10 g), alkalinized to pH 9-10 with NaOH 50% w/w and left under stirring for 30 minutes, then diluted with toluene (30 ml). The phases are separated and the aqueous phase is extracted with toluene (2×30 ml). The combined organic phases are dried over sodium sulfate and evaporated to dryness. The resulting oil is purified by flash chromatography (hexane/ethyl acetate 7:3). 0.48 g of product, as a pale yellow oil, are obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07420091B2uspto-grants-2008_09