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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549550Generated: October 29, 2026

4-(2-Propyn-1-yl)morpholine → {4-[3-Hydroxy-5-(3-morpholin-4-yl-prop-1-ynyl)-benzylsulfanyl]-2-methyl-phenoxy}-acetic acid ethyl ester

https://huagongshe.com/reaction/549550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Propyn-1-yl)morpholineHCID 412941—
Reactant[4-(3-Bromo-5-hydroxy-benzylsulfanyl)-2-methyl-phenoxy]-acetic Acid Ethyl EsterHCID 57791915—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product{4-[3-Hydroxy-5-(3-morpholin-4-yl-prop-1-ynyl)-benzylsulfanyl]-2-methyl-phenoxy}-acetic acid ethyl esterHCID 57791916—

Reaction Steps

[4-(3-Bromo-5-hydroxy-benzylsulfanyl)-2-methyl-phenoxy]-acetic acid ethyl ester (2.3 g; 5.6 mmol), 4-prop-2-ynyl-morpholine (2.1 g; 16.8 mmol), bis(triphenylphosphine)palladium (II) chloride (0.31 g; 0.45 mmol) and copper iodide (0.06 g; 0.34 mmol) were dissolved in a mixture of triethylamine (5 mL) and DMF (10 mL) under an atmosphere of nitrogen. The reaction mixture was reacted in a microwave oven at 100° C. for 1 h. The reaction mixture was purified by preparative HPLC (method A). Yield: 0.9 g. HPLC-MS: m/z: 456.1 (M+); Rt: 1.53 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943669B2
Source datasetuspto-grants-2011_05
ORD IDord-8cd34c61199d4b569466d1211724ebf3
Source noteuspto-grants-2011_05