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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815953Generated: October 30, 2026

N-bromobutanimide → 7-Bromo-1-[2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazol-6-ol

https://huagongshe.com/reaction/1815953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 135843648HCID 135843648—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-1-[2-(tert-butyldimethyl-silanyloxy)-propyl]-1H-indazol-6-olHCID 13584364966%

Reaction Steps

To a solution of the product from Step B (6.00 g, 19.6 mmol) in anhydrous THF (300 mL) at 0° C. was added N-bromosuccinimide (3.49 g, 19.6 mmol) in 10 portions over 20 min. The mixture was poured into a saturated aqueous solution of sodium bisulfite (300 mL) and extracted with EtOAc (3×100 mL). The combined extracts were dried (MgSO4) and evaporated to a residue (6.39 g). Chromatography (silica, 10% EtOAc/hexane) gave a solid (4.95 g, 66%): LC/MS (+APCI) m/z 385, 387 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881749B2
Source datasetuspto-grants-2005_04
ORD IDord-2f9b0c00c7af4141bea06275a35c0a4f
Source noteuspto-grants-2005_04