Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373614Generated: November 1, 2026

Isoamyl Nitrite → HCID 20093457, compound

https://huagongshe.com/reaction/373614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 20093436HCID 20093436—
SolventEthanolHCID 702—
ProductHCID 20093457HCID 20093457—

Reaction Steps

To a stirred solution of 5-butylamino-1,3-dimethylpyrazole (4.0 g, 23.9 mmol) in EtOH (100 mL) there was added dropwise, under nitrogen, isoamyl nitrite (35 mL) and the mixture was stirred at room temperature for 3 hours. The progress of the reaction was monitored by tlc (SiO2, developed with EtOAc/hexanes [3:2]) and when no starting material remained, the solution was evaporated to dryness. This mixture was purified by chromatography on a SiO2 column (400 mL) developed with EtOAc/hexanes (40:60). The faster components were eluted first (one of which is the isomeric N-nitroso derivative which can be isomerized with acid to yield additional product) followed by the Step C compound (3.23 g, 69%) as reddish crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164407
Source datasetuspto-grants-1992_11
ORD IDord-de849a6330c14b4ca8933481f99cb0ca
Source noteuspto-grants-1992_11