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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107059Generated: October 31, 2026

3-Methoxypropyne → HCID 23047376, compound

https://huagongshe.com/reaction/2107059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropyneHCID 69393—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 136364615HCID 136364615—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23047376HCID 23047376—

Reaction Steps

At room temperature under a protective gas, 1.4 ml of sodium hypochlorite solution is added dropwise to 155 mg of 5-benzyloxy-4-methoxymethyl-9-tosyl-β-carboline-3-carbaldehyde oxime hydrochloride in 6 ml of absolute tetrahydrofuran. The mixture is stirred until the oxime has disappeared (TLC control) for one hour at room temperature, then 210 mg of methylpropargyl ether is added dropwise and the mixture is agitated overnight at room temperature. After the solvent has been removed by distillation, the mixture is distributed in ethyl acetate/water, and the organic phase is dried over magnesium sulfate, filtered, and concentrated. The residue is dissolved in 8 ml of methanol, combined with 54 mg of sodium methylate, and heated to reflux for one hour. After concentration and distribution in ethyl acetate/concentrated sodium chloride solution, the organic phase is dried, filtered, and concentrated. The residue is chromatographed over silica gel with toluene+ethyl acetate in a ratio of 1:1. The corresponding fractions are combined and crystallized from ethyl acetate, thus obtaining 70 mg, melting point 133°-135° C. (ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933345
Source datasetuspto-grants-1990_06
ORD IDord-44892a9be4c44d6e9d28182287d3585c
Source noteuspto-grants-1990_06