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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910359Generated: October 31, 2026

Hydrogen Bromide → HCID 86093998, compound

https://huagongshe.com/reaction/1910359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 57674668HCID 57674668—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86093998HCID 8609399887%

Reaction Conditions

Temperature-13.5 °C

Reaction Steps

10.3 g (0.075 mol) of 2-amino-3,4,5-trimethylpyridine was added to 30 mL of 60% HBr. The mixture was cooled to −10 to −17° C. and pre-cooled 36.0 g (0.23 mol) bromine was added dropwise and the mixture was stirred for 20 mins. Pre-cooled (0° C.) NaNO2 solution of 13.5 g (0.19 mol) NaNO2 dissolved in 20 mL water was added dropwise into the reaction mixture at −10° C.˜−17° C. After addition, the reaction was stirred for one hour. Ice-cooled 25% NaOH solution was added slowly until the solution became basic. 200 mL of ethyl acetate was added to the mixture to extract the organic phase. The organic phase solvent was evaporated and the residue was distilled under vacuum. ˜13.1 g (87% yield) of the desired product was obtained which was confirmed by GC/MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08603645B2
Source datasetuspto-grants-2013_12
ORD IDord-c7955110fb43445ab0d035bb16d7c631
Source noteuspto-grants-2013_12