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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754112Generated: October 28, 2026

Triethylamine → N-(4-((3-(trifluoromethoxy)phenyl)sulfonyl)phenyl)acetamide

https://huagongshe.com/reaction/1754112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2734385—
ReactantSodium 4-acetamidobenzene-1-sulfinateHCID 23666794—
CatalystCupric acetateHCID 8895—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
ProductN-(4-((3-(trifluoromethoxy)phenyl)sulfonyl)phenyl)acetamideHCID 7097899857.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of sodium 4-acetamidobenzenesulfinate dehydrate (128 mg, 0.5 mmol), 3-trifluoromethoxy-phenylboronic acid (144 mg, 0.75 mmol) and Et3N (0.313 mL, 2.25 mmol) in 1,4-dioxane (4 mL) and DMSO (4 mL) is added Cu(OAc)2 (114 mg, 0.625 mmol). The mixture is heated at 60° C. for 16 h then cooled to ambient temperature. EtOAc (12 ml) and brine (6 ml) is added followed by concentrated NH4OH (0.6 mL) and the mixture is stirred at ambient temperature for 15 min. The layers are separated and the aqueous layer is extracted with EtOAc (6 mL). The combined extracts are dried (Na2SO4) and evaporated. The residue is purified by preparative TLC with 2:1 EtOAc/hexanes to give 104 mg (57%) white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169209B2
Source datasetuspto-grants-2015_10
ORD IDord-8008021cc14c4081b4213b819b0bdec4
Source noteuspto-grants-2015_10