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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469158Generated: November 1, 2026

Propargyl alcohol → HCID 178463301, compound

https://huagongshe.com/reaction/1469158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantDiisopropylamineHCID 7912—
ReactantHCID 178463214HCID 178463214—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
ProductHCID 178463301HCID 17846330163.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of methyl 5-bromo-3-(((trans)-4-((tert-butoxycarbonyl)(methyl)amino)cyclohexyl)(ethyl)amino)-2-methylbenzoate (2 g, 4.14 mmol) in dry toluene was added CuI (0.015 g, 0.079 mmol), PPh3 (0.043 g, 0.165 mmol), PdCl2(PPh3)2 (0.058 g, 0.082 mmol), N,N-diisopropyl amine (1.08 g, 10.78 mmol) and reaction was purged with argon for 15 min. prop-2-yn-1-ol (0.46 g, 8.29 mmol) was added to it reaction was heated at 80° C. at sealed condition for 5 h. On completion, it was quenched with water and extracted with ethyl acetate. Organic layer was dried over Na2SO4. The crude compound was purified by column chromatography to afford the title compound (1.2 g, 63.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006242B2
Source datasetuspto-grants-2015_04
ORD IDord-f9d00b1007a84423b0fdc450db2300a1
Source noteuspto-grants-2015_04