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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841098Generated: October 30, 2026

Potassium Carbonate → HCID 502055, compound

https://huagongshe.com/reaction/841098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
ReactantHCID 5494875HCID 5494875—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystZincchlorideHCID 3007855—
SolventDimethylformamideHCID 6228—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 502055HCID 50205527.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 7-propionate 7a (0.83 g, 3.0 mmol) in 2-butanone (40 mL) and DMF (4 mL) were added tetrabutylammonium iodide (1.11 g, 3 rnmol), K2CO3 (1.04 g, 7.5 mmol), and 3-chloro-3-methyl-1-butyne (1.11 g, 3 mmol). The reaction mixture was heated at 60° C. for 1 h before ZnCl2 (3.9 mL of 1.0 M solution in ether, 3.9 mmol) was added. The temperature was then raised to 70° C. and maintained at that temperature for 21 h. The reaction mixture was cooled to room temperature and quenched with saturated aqueous NH4Cl (100 mL). The mixture was extracted with EtOAc (100 mL×2) and the combined organic layers were washed with brine (100 mL) and dried over Na2SO4. Evaporation of the solvent gave the crude product (1.9 g). After column chromtographic purification, 280 mg (27.1% yield) of the desired product 5a was obtained as a waxy solid. 1H NMR (DMSO-d6) 1.00 (3H, t, J=7.2 Hz), 1.16 (3H, t, J=7.5 Hz); 1.47 (6H, s), 1.61 (2H, m), 2.71 (2H, q, J=7.5 Hz), 2.89 (2H, t, J=7.8), 5.84 (1H, d, J=9.9 Hz), 6.17 (1H, s), 6.41 (1H, d, J=10.2 Hz); 13C NMR (DMSO-d6) 8.6, 13.7, 22.8, 26.6, 27.2, 37.4, 78.3, 103.6, 107.2, 110.8, 113.4, 115.5, 130.1, 148.5, 151.4, 154.4, 156.9, 159.3, 172.2; IR 1767 (s and sharp), 1723 (s and sharp), 1616 (s and sharp) cm−1; MS m/e 343 (M+1); Anal. Calcd. for C20H22O5: C, 70.16; H, 6.47. Found: C, 70.37; H, 6.51.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369241B1
Source datasetuspto-grants-2002_04
ORD IDord-df3ee4ff4e2e4ecbb50f4e8bcaf68f69
Source noteuspto-grants-2002_04