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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633469Generated: October 30, 2026

Hydrochloric Acid → 2,3,5-Trichlorophenylboronic acid

https://huagongshe.com/reaction/1633469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-2,3,5-trichlorobenzeneHCID 4382903—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product2,3,5-Trichlorophenylboronic acidHCID 5106508—

Reaction Steps

A solution of 2,3,5-trichlorobromobenzene (8.60 g, 0.033 mole) in dry ether (33 ml) and bromoethane (4.73 ml, 7.31 g, 0.067 mole) was added dropwise to a suspension of magnesium turnings (2.80 g, 0.12 mole) in dry ether (21.50 ml) at room temperature. The mixture was refluxed for 0.50 hr and cooled to room temperature. The mixture was then added dropwise under nitrogen to a solution of trimethylborate (5.16 ml, 5.16 g, 0.05 mole) in dry ether (8.60 ml) maintaining the temperature below −60° C. This was warmed to room temperature overnight, then cooled in an ice-bath and treated with 2M hydrochloric acid (10 ml). The ether layer was separated, washed with water (2×20 ml), dried over anhydrous magnesium sulphate, filtered and the filtrate evaporated in vacuo. The residue was triturated with 40-60° C. petroleum ether, filtered and dried in vacuo. Yield 4.57 g (61%), M.p. 257-260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503909B1
Source datasetuspto-grants-2003_01
ORD IDord-4aeb942a571146eeae9f6871027b11f2
Source noteuspto-grants-2003_01