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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112148Generated: November 1, 2026

Trimethyl borate → HCID 67410628, compound

https://huagongshe.com/reaction/2112148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantHCID 67409251HCID 67409251—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67410628HCID 6741062852%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-Bromo-1-[3-(tert-butyl-diphenylsilanyloxy)-propyl]-1H-indazole (3s) (200 mg, 0.41 mmol) was dissolved in 4.0 mL THF and cooled to −78° C. A solution of n-butyl lithium in hexanes (2.5M, 0.17 mL) was added slowly. The yellow solution was stirred for 30 minutes. Trimethyl borate (130 mg, 1.2 mmol) was added and the reaction was warmed to room temperature and stirred for 30 min. The reaction was quenched with 10 mL of a 0.3% aqueous HCl solution and the resulting mixture was stirred for 30 min. The reaction was diluted with Et2O and the layers were separated. The organic phase was washed with brine. The aqueous phases were extracted once with Et2O. The organic phases were combined, dried (MgSO4), filtered, and concentrated in vacuo. The crude product was partially purified on silica gel with 3% MeOH/CH2Cl2 to afford (4s) (97 mg, 52%). MS (ESI+) m/z 459 (M+H)+. HPLC (5 to 95%) 3.74 min. This mixture was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521447B2
Source datasetuspto-grants-2009_04
ORD IDord-38bdc185b7d849c8a66c854b9efb45f9
Source noteuspto-grants-2009_04