HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetamide → 2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Reactant | Sodium hydrogencarbonate brine | HCID 129703874 | — |
| Product | 2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide | HCID 86628475 | — |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895782B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-c75fc2d63c674a13b2c16a843f41fd3e |
| Source note | uspto-grants-2014_11 |