Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169621Generated: October 30, 2026

Hydrochloric Acid → 2-Formyl-3-thiopheneboronic acid

https://huagongshe.com/reaction/1169621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(3-Bromothiophen-2-yl)-1,3-dioxolaneHCID 12220211—
Reactantn-ButylborateHCID 86592051—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product2-Formyl-3-thiopheneboronic acidHCID 277342650.2%

Reaction Steps

A 1.1 N solution of n-butyllithium in hexane (28 ml) was added dropwise (10 mins) to a solution of 2-(3-bromo-2-thienyl)-1,3-dioxalane (3) (6.6 g, 28.1 mmol) in anhydrous ether (30 ml) at −70° C. After stirring for 10 mins, butyl borate (9.1 ml, 33.7 mmol) in anhydrous ether (20 ml) was added in a single portion. The reaction mixture was stirred for 4 hrs at −70° C. and then left to return to room temperature. 1 N hydrochloric acid (20 ml) was added, and the mixture was left for 1 hr with stirring. The aqueous phase was extracted with ether and the combined ether phases were washed with a solution of sodium bicarbonate, dried (Na2SO4), and evaporated under reduced pressure to give the intermediate (4) (2.2 g, 14.1 mmol, 50% yield) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825129B2
Source datasetuspto-grants-2010_11
ORD IDord-08317676157643a49cdf00b0aadda43c
Source noteuspto-grants-2010_11