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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Benzo[b]thiophene-4-carboxylic acid | HCID 1051638 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Carboxybenzo[b]thiophen-2-yl)boronic acid | HCID 67272237 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863302B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-0acf80ccbd0c42a4a68f85c323069aac |
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| Source note | uspto-grants-2011_01 |
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