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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307541Generated: October 25, 2026

Hydrochloric Acid → (3-(Methoxymethoxy)phenyl)boronic acid

https://huagongshe.com/reaction/2307541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant3-BromophenolHCID 11563—
ReactantTriisopropyl borateHCID 21531—
ReactantSodium hydrideHCID 24758—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product(3-(Methoxymethoxy)phenyl)boronic acidHCID 22606941—

Reaction Conditions

Temperature-78 °C

Reaction Steps

10 g (57.8 mmol) of 3-bromophenol are dissolved in 150 mL of anhydrous DMF. 2.55 g (63.6 mmol) of 60% sodium hydride are then added and the reaction medium is stirred for 1 hour. 4.83 mL (63.6 mmol) of methoxymethyl chloride are then added dropwise and the reaction mixture is stirred for 1 h. After treatment with saturated ammonium chloride solution, extraction with ethyl ether and evaporation of the solvents from the organic phase, the residue obtained is dissolved in 200 mL of anhydrous THF. The mixture is cooled to −78° C. and 25.4 mL (63.6 mmol) of 2.5M butyllithium solution are then added. After stirring for 1 hour at −78° C, 15 mL (65 mmol) of triisopropyl borate are added dropwise. The reaction medium is stirred for 1 hour and then warmed to room temperature, after which it is treated with 1N hydrochloric acid solution. The medium is then extracted with ethyl acetate, after which the organic phases are combined, dried and then concentrated under reduced pressure. After slurrying in heptane and then concentration, a brown solid is obtained (m.p.=45° C., m=5.8 g; Y=67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831106B1
Source datasetuspto-grants-2004_12
ORD IDord-2a1878b61ce64b768ebcd2649e3b77cb
Source noteuspto-grants-2004_12