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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218853Generated: October 29, 2026

Propyne → HCID 67286863, compound

https://huagongshe.com/reaction/218853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyneHCID 6335—
ReactantHCID 67286648HCID 67286648—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventTriethylamineHCID 8471—
ProductHCID 67286863HCID 6728686367.3%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A mixture of the product of Step A (0.123 g; 0.296 mmol), Cl2Pd(PPh3)2 (0.040 g; 0.057 mmol), CuI (0.014 g; 0.073 mmol) in anhydrous triethylamine (3 ml) was cooled to −40° C., degassed under reduced pressure and saturated with dry N2. The propyne gas (0.45 g; 11.2 mmol) was added to it at −40° C. The reaction flask was sealed with septum and allowed to warm up to room temperature and stirred for 3 h at room temperature and diluted to 20 ml with diethyl ether and solid precipitated, filtered off. The filtrate was evaporated to dryness under reduced pressure and the residue, purified by flash column chromatography (SiO2, hexane, hexane/ethyl acetate, 9:1) to give the title compound (0.065 g; 67% yield) as colourless syrup. 1H-NMR (CDCl3) 1.26 (d, 6H, J=6.17 Hz); 2.09 (s, 3H); 3.79 (s, 3H); 4.2 (s, 2H); 4.44 (m, 1H, J=6.17 Hz); 6.73 (d, 1H, J=8.53 Hz); 7.12 (d, 1H, J=8.53 Hz); 7.15-7.4 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198466B2
Source datasetuspto-grants-2012_06
ORD IDord-956283c55a144f30bf6bc81d394aeab6
Source noteuspto-grants-2012_06