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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726878Generated: October 27, 2026

Hydrochloric Acid → 4-(Morpholin-4-ylsulphonyl)benzeneboronic acid

https://huagongshe.com/reaction/1726878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant4-(4-Iodophenyl)sulfonylmorpholineHCID 3800223—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(Morpholin-4-ylsulphonyl)benzeneboronic acidHCID 44119546—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 25 g of the compound obtained in Step A (70.8 mmol) and 26 ml of triisopropyl borate in 400 ml of THF cooled to −60° C. there are added, dropwise, over 45 minutes and under a gentle current of nitrogen, 53 ml of a 1.6M solution of BuLi (84.9 mmol) in hexane. The reaction solution is then stirred for 1 hour 30 minutes at −60° C. and is subsequently returned to ambient temperature over 2 hours. The reaction mixture is treated with about 100 ml of 1N HCl and is extracted 3 times with ethyl acetate. The organic phases are collected, washed with brine, dried (MgSO4) and evaporated under reduced pressure. The residue obtained is chromatographed on an SiO2 column, eluting with CH2Cl2 and then with a mixture of CH2Cl2/MeOH 98/2 and then 95/5. After evaporation of the fractions, the residue is triturated in ethyl ether to yield the title product after filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494994B2
Source datasetuspto-grants-2009_02
ORD IDord-e0f2c65fff144a3a921563260a6639e6
Source noteuspto-grants-2009_02