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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946631Generated: November 3, 2026

Triethylamine → methyl 4-(3-(11-oxodibenzo[b,f][1,4]oxazepin-10(11H)-yl)prop-1-ynyl)benzoate

https://huagongshe.com/reaction/1946631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 4-iodobenzoateHCID 69273—
Reactant10-(prop-2-ynyl)dibenzo[b,f][1,4]oxazepin-11(10H)-oneHCID 59783448—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Productmethyl 4-(3-(11-oxodibenzo[b,f][1,4]oxazepin-10(11H)-yl)prop-1-ynyl)benzoateHCID 5978365560%

Reaction Steps

The title compound 434 (0.310 g, 1.24 mmol) and the methyl 4-iodobenzoate (0.390 g, 1.48 mmol) were stirred in acetonitrile (10.0 mL). Copper iodide (24 mg, 0.124 mmol) and dichlorobis(triphenylphosphine)palladium (87 mg, 0.124 mmol) were added followed by triethylamine (0.44 mL, 3.11 mmol). The reaction mixture was stirred at room temperature for 4 hours. The mixture was poor into ethyl acetate and the organic layer was washed with water and brine, dried over sodium sulfate, filtered and evaporated. The crude was purified by flash chromatography (10-30% ethyl acetate in hexanes) to afford title compound 435 (285 mg, 60%) as a light brown solid. MS (m/z): 384.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399452B2
Source datasetuspto-grants-2013_03
ORD IDord-c3b2eb97682848ba9d4fcab2044cc559
Source noteuspto-grants-2013_03