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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219951Generated: October 26, 2026

2-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → Methyl 2-fluoro-4-{5-[2'-methoxy-2-(methoxymethyl)biphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoate

https://huagongshe.com/reaction/219951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11402049—
Reactant3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acidHCID 21947812—
ReactantMethyl 4-{5-[4-bromo-3-(methoxymethyl)phenyl]-1,2,4-oxadiazol-3-yl}-2-fluorobenzoateHCID 67528348—
ProductMethyl 2-fluoro-4-{5-[2'-methoxy-2-(methoxymethyl)biphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoateHCID 67528482—

Reaction Steps

Title compound was prepared following procedure and work up described for Intermediate 5 step 2 but starting from methyl 4-{5-[4-bromo-3-(methoxymethyl)phenyl]-1,2,4-oxadiazol-3-yl}-2-fluorobenzoate obtained from step 1 (50 mg, 0.12 mmol) and 2-(2-methoxy-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (30.5 mg, 0.13 mmol) (130° C. for 10 min under microwave irradiation). Purification by flash chromatography (cHex:EtOAc, from 100:0 to 20:80) gave the title compound as a yellow powder. LC/MS (Method B): 449.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-d5834a286fdf49d09123732e338233a8
Source noteuspto-grants-2012_06