تفاعل #428817

ord-c75fc2d63c674a13b2c16a843f41fd3e

معادلة التفاعل

NC(=O)C(F)(F)F
THP-phenol
NC(=O)C(F)(F)F
trifluoroacetamide
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
C1CCOC1.O
THF H2O
O.O=C([O-])O.[Cl-].[Na+].[Na+]
NaHCO3 brine
O=C(NCCCCc1cccc(O)c1)C(F)(F)F
2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwere separated
  2. 2
    استخلاصaqueous layer extracted with EtOAc
  3. 3
    غسيلCombined organic layers were washed with brine
  4. 4
    تركيزconcentrated under reduced pressure
  5. 5
    أخرىPurification by flash chromatography (10%-50% EtOAc-hexanes gradient)

الإجراء التجريبي

A mixture of THP-phenol 136 (0.72 g, 2.08 mmol), p-toluenesulfonic acid monohydrate (0.366 g) in THF:H2O (3:1, 20 mL) was stirred at room temperature for 3.5 hr. The reaction mixture was treated with aqueous NaHCO3-brine solution, layers were separated and aqueous layer extracted with EtOAc. Combined organic layers were washed with brine and concentrated under reduced pressure. Purification by flash chromatography (10%-50% EtOAc-hexanes gradient) gave 2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide as a colorless oil, which was taken into the next step. Yield (0.438 g, 96%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08895782B2uspto-grants-2014_11