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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyl borateHCID 12712—
Reactant4-Bromo-5-isopropyl-1H-indazoleHCID 22566916—
ReactantHCID 178506859HCID 178506859—
SolventDiethyl EtherHCID 3283—
Product(5-Isopropyl-1H-indazol-4-yl)boronic acidHCID 57358541—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338591B2
Source datasetuspto-grants-2012_12
ORD IDord-a7aa638c09c84a729b4a7ddc0e84acf9
Source noteuspto-grants-2012_12