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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417836Generated: November 1, 2026

Propargyl alcohol → Methyl 2-(3-hydroxyprop-1-yn-1-yl)benzoate

https://huagongshe.com/reaction/1417836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantBenzoic acid, 2-iodo-, methyl esterHCID 69132—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
ProductMethyl 2-(3-hydroxyprop-1-yn-1-yl)benzoateHCID 4321316—

Reaction Steps

Step 1--A mixture of methyl o-iodobenzoate (9.17 g), propargyl alcohol (3.06 ml) and diethyl amine (90 ml) is treated with bis(triphenylphosphine)palladium chloride (1.23 g) and copper iodide (333 mg) and the reaction is stirred at 20°-25° under nitrogen for 18 hrs. The reaction is then filtered through a filter agent and concentrated. The resulting residue is partitioned between water and dichloromethane. The combined organic phases are washed once with saline, dried over magnesium sulfate, filtered and concentrated to an oil. Purification by silica gel chromatography gives methyl o-(1-hydroxy-2-propyn-3-yl)benzoate (CXIX).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877317
Source datasetuspto-grants-1999_03
ORD IDord-7078d2e282ea4def9eba75df7b340ae7
Source noteuspto-grants-1999_03