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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969482Generated: October 27, 2026

Potassium Carbonate → Ethyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate

https://huagongshe.com/reaction/969482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 2-fluoro-, ethyl esterHCID 67953—
ReactantTert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamateHCID 69643261—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductEthyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoateHCID 21911050104.9%

Reaction Steps

2.15 g (12.8 mmol) of ethyl 2-fluorobenzoate and 1.9 g (14 mmol) of potassium carbonate are successively added to a solution of 4 g (12.8 mmol) of tert-butyl (4′-hydroxybiphenyl-3-ylmethyl)methylcarbamate in 45 ml of dimethylacetamide. The reaction medium is refluxed for 48 hours, cooled, diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 3.1 g of ethyl 2-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate are obtained in the form of a colorless oil, in a yield of 53%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307078B2
Source datasetuspto-grants-2007_12
ORD IDord-cb2bf88750c64ea8856627e28cf92620
Source noteuspto-grants-2007_12