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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640794Generated: October 29, 2026

Benzyl Bromide → HCID 59256698, compound

https://huagongshe.com/reaction/640794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 135412675HCID 135412675—
SolventEthanolHCID 702—
ProductHCID 59256698HCID 5925669847%

Reaction Steps

A mixture of 6,8-dichloro-3-methylquinoxalin-5-ol (150 mg, 0.655 mmol), benzyl bromide (0.20 mL, 1.68 mmol), KOH (0.09 g) and EtOH (10 mL) was heated under reflux for 16 h, cooled, and concentrated. Dichloromethane (20 mL) was added and the mixture washed with H2O (5 mL×2), dried and concentrated. The residue was purified via SiO2-gel chromatography (dichloromethane/MeOH, 1:0-150:1) to give 8-benzyloxy-5,7-dichloro-2-methylquinoxaline (98 mg, 47%).—1H NMR (CDCl3): δ 8.82 (s, 1H), 7.81 (s, 1H), 7.58 (m, 2H), 7.38 (m, 2H), 5.45 (s, 2H), 2.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692011B2
Source datasetuspto-grants-2010_04
ORD IDord-a0ecb9e73bea402a8bb68527d738a5b6
Source noteuspto-grants-2010_04