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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475742Generated: November 1, 2026

Hydrochloric Acid → 4-Borono-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl Ester

https://huagongshe.com/reaction/1475742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
ReactantBis(dimethylaminoethyl) etherHCID 18204—
Reactant4-Iodo-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl EsterHCID 67170900—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product4-Borono-3-(2-m-tolyl-ethoxy)-benzoic Acid Methyl EsterHCID 6716956256.4%

Reaction Conditions

Temperature15 °C

Reaction Steps

2.3 g of bis(2-dimethylaminoethyl)ether were dissolved in 50 ml of anhydrous THF and 7.1 ml of a 2 M solution of isopropylmagnesium chloride added at 15° C. The mixture was stirred for 20 min at 15° C. Then a solution of 4.7 g of 4-iodo-3-(2-m-tolyl-ethoxy)-benzoic acid methyl ester in 20 ml of anhydrous THF was added at room temperature. The mixture was stirred for 10 min at 20° C., and then 2.4 g of trimethyl borate were added dropwise at 0° C. and the mixture stirred for 20 min at 0° C. 100 ml of 0.1 N hydrochloric acid were added, and the mixture was extracted three times with 100 ml of EA. The combined organic layers were washed with 100 ml of water, dried with magnesium sulfate and evaporated. Silica gel chromatography (EA/HEP 1:5) of the residue yielded 2.1 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018383B2
Source datasetuspto-grants-2015_04
ORD IDord-b7657db27738465781aaea1dbce2eceb
Source noteuspto-grants-2015_04