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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250241Generated: November 1, 2026

Diisopropylamine → (4-Carboxybenzo[b]thiophen-2-yl)boronic acid

https://huagongshe.com/reaction/250241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTriisopropyl borateHCID 21531—
ReactantBenzo[b]thiophene-4-carboxylic acidHCID 1051638—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-Carboxybenzo[b]thiophen-2-yl)boronic acidHCID 6727223796%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of n-BuLi (2.5M in hexane, 1.69 mol, 676 mL) is added slowly at −78° C. to a solution of diisopropylamine (1.69 mol, 236 mL) in 2 L of anhydrous THF. The mixture is stirred for 30 min. A solution of benzo[b]thiophene-4-carboxylic acid (0.8 mol, 143 g) in 2 L of anhydrous THF is added slowly and the mixture is allowed to reach 0° C. The reaction is cooled to −30° C. and the triisopropyl borate (2 mol, 463 mL) is added slowly. The cooling bath is removed and the mixture is allowed to reach room temperature. The reaction is quenched with 1.3 L of concentrated HCl and 1 L of water. The mixture is stirred overnight. The organic solvent is removed under reduced pressure. The precipitate is collected by filtration, washed with water, and dried under vacuum to yield the title compound (170.5 g, 96%). ES/MS m/e 221 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863302B2
Source datasetuspto-grants-2011_01
ORD IDord-0acf80ccbd0c42a4a68f85c323069aac
Source noteuspto-grants-2011_01