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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619146Generated: October 26, 2026

Hydrochloric Acid → 2-Methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenylboronic acid

https://huagongshe.com/reaction/1619146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(3-Iodo-4-methylphenyl)-5-methyl-1,3,4-oxadiazoleHCID 58170497—
ReactantHCID 178418918HCID 178418918—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenylboronic acidHCID 5817051666.2%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Isopropylmagnesium chloride (2.0 M in tetrahydrofuran, 10 mL, 20.0 mmol) was added dropwise over 20 minutes to a stirred solution of 2-(3-Iodo-4-methylphenyl)-5-methyl-1,3,4-oxadiazole (preparation 55c, 4.0 g, 13.3 mmol) in tetrahydrofuran (40 mL) at −10° C. The mixture was stirred for 1 hour at −10° C. then triisopropyl borate (4.71 mL, 20.0 mmol) was added dropwise over 10 minutes and the mixture was stirred for 1 hour at −10° C. Then, the mixture was warmed to room temperature and stirred overnight. Water was then added, the mixture was cooled by means of an ice-water bath and the pH was adjusted to 3-4 with 2M aqueous hydrochloric acid. The mixture was extracted with ethyl acetate and the organic layer was washed with brine, dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and the solid was filtered and dried to give the title compound (1.92 g, 66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772288B2
Source datasetuspto-grants-2014_07
ORD IDord-0e206c4966e34cfab2b460caa8cb5285
Source noteuspto-grants-2014_07