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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936238Generated: October 26, 2026

3-Methyl-1-pentyn-3-ol → 3-Cyclopentyl-2-[4-(3-hydroxy-3-methyl-pent-1-ynyl)-phenyl]-propionic acid methyl ester

https://huagongshe.com/reaction/1936238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-1-pentyn-3-olHCID 6494—
Reactant3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl esterHCID 67483447—
CatalystTriethylamineHCID 8471—
CatalystIodide IonHCID 30165—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
Product3-Cyclopentyl-2-[4-(3-hydroxy-3-methyl-pent-1-ynyl)-phenyl]-propionic acid methyl esterHCID 67484106102.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (716 mg, 2.0 mmol) and triethylamine (2 mL, 0.01 mmol) in N,N-dimethylformamide (2 mL) was treated with 3-methyl-1-pentyn-3-ol (0.56 mL, 5.0 mmol). The resulting reaction mixture was degassed with argon and then treated with cooper iodide (10 mg, 0.05 mmol) and bis(triphenylphosphine)palladium (II) chloride (15 mg, 0.02 mmol). The reaction was then heated at 70° C. for 24 h. At this time, the reaction was cooled to 25° C. and concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and a half-saturated aqueous sodium chloride solution (1×20 mL). The aqueous layer was back extracted with ethyl acetate (1×40 mL). The combined organic extracts were washed with a half-saturated aqueous sodium chloride solution (1×20 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 ethyl acetate/hexanes) afforded 3-cyclopentyl-2-[4-(3-hydroxy-3-methyl-pent-1-ynyl)-phenyl]-propionic acid methyl ester (673 mg, 98%) as an orange oil: EI-HRMS m/e calcd for C21H28O3 (M+) 328.2038, found 328.2040.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388071B2
Source datasetuspto-grants-2002_05
ORD IDord-6996b5b620e645c8ba6a80ab63d04a44
Source noteuspto-grants-2002_05