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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209463Generated: October 30, 2026

Trimethyl borate → (3-Chlorophenyl)boronic acid

https://huagongshe.com/reaction/2209463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantHCID 21749248HCID 21749248—
SolventEthyl AcetateHCID 8857—
Product(3-Chlorophenyl)boronic acidHCID 2734323—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of trimethylborate in 200 mL of ethyl acetate was cooled to -65° C. 3-Chlorobenzene magnesium chloride (0.8M, 60 mL), i.e., a grignard reagent, was added to the solution in a dropwise manner over 20 minutes. The mixture was kept in the temperature range of -60° C. to -70° C. and stirred. After 30 minutes, the mixture was allowed to warm to 0° C. and stirred for 1 hour. The mixture was quenched with H2O (25 mL) and stirred at room temperature for 1 hour. The solvent was removed and the remaining mass was extracted ethyl ether (3×100 mL). The organic layers were combined and washed with H2O (2×50 mL), dilute HCl (2×100 mL), H2O (2×50 mL) and brine (1×50 mL). The organic layer was dried with MgSO4, concentrated and allowed to stand. 100 mL of hexanes was added and the solution was stirred for 1 hour. The solution was filtered and allowed to air dry yielding 4.6 g of 3-chlorobenzene boronic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455252
Source datasetuspto-grants-1995_10
ORD IDord-d9ae3bb05887444f96e25c632c39d472
Source noteuspto-grants-1995_10