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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29374Generated: October 27, 2026

Morpholine → 3-Methyl-4-morpholin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/29374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl esterHCID 86599030—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product3-Methyl-4-morpholin-4-yl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871545360.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

To 3-methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester (190 mg, 0.5 mmol) was added K3PO4 (159 mg, 0.75 mmol), morpholine (52 mg, 0.6 mmol), Pd(OAc)2 (10 mg) and 4 mL of dioxane. The mixture was heated and stirred in an 85° C. oil bath overnight. The reaction mixture was poured into water and was extracted with ethyl acetate. The organic extract was washed with water and dried over sodium sulfate. Removal of the solvent in vacuo gave the crude product, which was purified by column chromatography to give 96 mg of 3-methyl-4-morpholin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester, obtained as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-8239c2520776414b9a2e6b0f56193e44
Source noteuspto-grants-2008_09