Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162147Generated: October 25, 2026

Isobutyl nitrite → 5-bromo-1H-indazole

https://huagongshe.com/reaction/1162147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl nitriteHCID 10958—
Reactant3-Amino-5-bromo-1H-indazoleHCID 817910—
ReactantPhosphinic AcidHCID 4124402—
SolventEthanolHCID 702—
Product5-bromo-1H-indazoleHCID 76192940.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3-amino-5-bromo-indazole, (4.60 g, 22 mmol) and ethanol (50 mL) was treated with hypophosphorous acid (50% aqueous solution, 9.6 ml, 87 mmol) and cooled to 0° C. To the reaction mixture was added isobutyl nitrite (2.6 mL, 22 mmol). The mixture was warmed to room temperature and the yellow suspension was stirred for two hours. The resulting brown suspension was treated with isobutyl nitrite (1 mL) and stirred at room temperature for one hour. The reaction was quenched with brine (100 mL) and the mixture extracted with ethyl acetate (2×100 mL). The combined organic layers were dried over magnesium sulfate, filtered and evaporated to a brown oil which was purified by chromatography using silica gel and hexane/ethyl acetate to give 5-bromo-indazole as a tan solid (1.74 g, 40%): mp 122-124° C.; MS [M+H]+ 195, 197.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820670B2
Source datasetuspto-grants-2010_10
ORD IDord-2a234837d2824214a222fe395847aefd
Source noteuspto-grants-2010_10