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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186317Generated: November 2, 2026

4-Methoxybenzyl alcohol → HCID 67401255, compound

https://huagongshe.com/reaction/1186317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloroquinoxalin-2-amineHCID 817274—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67401255HCID 6740125576%

Reaction Steps

According to Step 2 of Reference Example 7-1, by use of 4-methoxybenzyl alcohol (625 μL, 5.01 mmol), 60% sodium hydride (in oil) (200 mg, 5.01 mmol), tetrahydrofuran (6.0 mL) and 2-amino-3-chloroquinoxaline (300 mg, 1.67 mmol), the mixture was stirred and reacted at room temperature for 17 hours. Then, slurry purification was performed using diisopropyl ether, to give 2-amino-3-[(4-methoxyphenyl)methoxy]quinoxaline (Compound BB) (357 mg, yield: 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-8f320b2adcbb41ac99be93aa47d8f654
Source noteuspto-grants-2014_03