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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377254Generated: October 25, 2026

Triethylamine → Phenyl 5-(3-phenoxy-1-propynyl)-3-thiophenecarboxylate

https://huagongshe.com/reaction/2377254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant(Prop-2-ynyloxy)benzeneHCID 83613—
ReactantPhenyl 5-bromothiophene-3-carboxylateHCID 58591683—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductPhenyl 5-(3-phenoxy-1-propynyl)-3-thiophenecarboxylateHCID 16220355—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of phenyl 5-bromothiophene-3-carboxylate, Example 113 (100 mg, 0.35 mmol), (prop-2-ynyloxy)benzene (93 mg, 0.71 mmol), triphenylphosphine (19 mg, 0.071 mmol), dichlorobis(triphenylphosphine)palladium(II) (12 mg, 0.018 mmol), copper iodide (1 mg, 0.006 mmol) and triethylamine (0.74 mL, 5.30 mmol) in N,N-dimethylformamide (1 mL) was stirred under nitrogen in a heavy walled process vial in a microwave synthesizer at about 120° C. for about 25 minutes. The reaction mixture was concentrated under vacuum and the residue was purified by flash column chromatography on silica gel using hexane/ethyl acetate (2:1) as the mobile phase to provide the desired product. MS (DCI-NH3): m/z 352 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468371B2
Source datasetuspto-grants-2008_12
ORD IDord-8c1c44f128624e6d9e7e013a7fe9f2b8
Source noteuspto-grants-2008_12