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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517171Generated: October 26, 2026

Trifluoroacetamide → 2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide

https://huagongshe.com/reaction/517171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetamideHCID 67717—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantOxolane--water (1/1)HCID 21881883—
ReactantSodium hydrogencarbonate brineHCID 129703874—
Product2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115056B2
Source datasetuspto-grants-2015_08
ORD IDord-38f3a3320adf4afca65b573a9cfd8404
Source noteuspto-grants-2015_08