HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197404Generated: October 29, 2026
Tributyl borate → (5-Isopropyl-1H-indazol-4-yl)boronic acid
https://huagongshe.com/reaction/2197404
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | 4-Bromo-5-isopropyl-1H-indazole | HCID 22566916 | — |
| Reactant | HCID 178506859 | HCID 178506859 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (5-Isopropyl-1H-indazol-4-yl)boronic acid | HCID 57358541 | — |
Reaction Steps
A solution of 4-bromo-5-isopropyl-1H-indazole (1.6 g, 6.9 mmol) in Et2O (4 mL) is added slowly to a suspension of KH (1.0 g of 30% dispersion in mineral oil, 7.7 mmol) in Et2O (20 mL) at 0° C. and the mixture is stirred for 20 min. After cooling to −78° C., i-BuLi (8.9 mL of 1.7 M in Hex, 15 mmol) is added and the resulting mixture is stirred for 40 min at −78° C. To this is added B(On-Bu)3 (5.6 mL, 21 mmol) and the mixture is stirred for 24 h at room temperature. The reaction mixture is quenched with 1N H3PO4 and extracted with Et2O. The combined Et2O layers are back-extracted with 1N NaOH (3×10 mL). The combined NaOH extracts are acidified with 1N H3PO4 and extracted with EtOAc. The EtOAc extracts are washed with saturated brine, dried (MgSO4), and concentrated to yield 5-isopropyl-1H-indazole-4-boronic acid. 1H NMR (CDCl3) 7.85 (s, 1H), 7.42 (d, 1H), 7.37 (d, 1H), 3.6 (br s, 2H), 2.88 (m, 1H), 1.32 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338591B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a7aa638c09c84a729b4a7ddc0e84acf9 |
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| Source note | uspto-grants-2012_12 |
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