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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348822Generated: October 27, 2026

Trimethylsilylacetylene → Methyl 3-[(dipropylamino)carbonyl]-5-ethynylbenzoate

https://huagongshe.com/reaction/348822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl 3-bromo-5-(dipropylcarbamoyl)benzoateHCID 21939662—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductMethyl 3-[(dipropylamino)carbonyl]-5-ethynylbenzoateHCID 21086178111.3%

Reaction Steps

A mixture of methyl 3-bromo-5-[(dipropylamino)carbonyl]benzoate (XXI, 200 mg, 0.58 mmol), PdCl2(Ph3P)2 (16 mg, 0.03 mol %) and copper (I) iodide (6 mg, 0.05 mol %) in triethylamine (1.2 mL) is heated to reflux. (Trimethylsilyl) acetylene (100 microliter, 0.7 mmol) is added, and the mixture stirred for 3 hours, cooled to 20–25 degrees, diluted with water (20 mL), and extracted with chloroform (3×15 mL). The combined organic extracts are washed with saline (20 mL), dried over sodium sulfate and concentrated under reduced pressure to give methyl 3-[(dipropylamino)carbonyl]-5-ethynylbenzoate (XXXII, 185.5 mg), NMR (300 MHz, CDCl3): δ 7.95, 7.75, 7.43, 3.74, 3.25, 2.95, 1.49, 1.34, 0.79, 0.56 and 0.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-3b64db1550d0401ba1756e8d053d8bb7
Source noteuspto-grants-2007_02