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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705474Generated: October 28, 2026

Triethylamine → HCID 68181951, compound

https://huagongshe.com/reaction/705474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
ReactantHCID 570771HCID 570771—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
ProductHCID 68181951HCID 68181951—

Reaction Conditions

Temperature120 °C

Reaction Steps

4-iodobenzotrifluoride (150 μL, 1 mmol), phenylpent-1-en-4-yn-3-ol (190 mg, 1.2 mmol), bis(triphenylphosphine)palladium(II) dichloride (14 mg, 0.02 mmol), copper iodide (3 mg, 0.03 mmol) and triphenylphosphine (52 mg, 0.2 mmol) were introduced in a 10 mL microwave vial flushed with argon. This was diluted with anhydrous triethylamine (700 μL, 4 mmol) in anhydrous degased 1,4-dioxane (1.3 mL). The solution was heated under microwave irradiation at 120° C. for 45 min. The reaction mixture was poured into a mix of 1M aqueous solution of hydrochloric acid (10 mL) and saturated aqueous ammonium chloride solution (10 mL), and this was extracted with dichloromethane (3×15 mL). The combined organic layers were dried over magnesium sulfate, filtered, and evaporated to dryness to give crude product which was purified by flash chromatography (SiO2, DCM/Hexanes 3:7). The resulting yellow solid was recrystallized (EtOH/Hexanes 1:3) to give pure final compound TG008A86 as a pale yellow powder (155 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174960B2
Source datasetuspto-grants-2015_11
ORD IDord-57d12df533a044c9968b192e1352b127
Source noteuspto-grants-2015_11