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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881174Generated: November 2, 2026

Ethanol → Benzothiazole, 5,6-dimethoxy-2-methyl-

https://huagongshe.com/reaction/1881174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium SulfideHCID 14804—
Reactant4-Bromo-5-nitroveratroleHCID 170968—
ReactantSulfurHCID 5362487—
ProductBenzothiazole, 5,6-dimethoxy-2-methyl-HCID 112829—

Reaction Steps

1-Bromo-4,5-dimethoxy-2-nitro-benzene (10 g) was suspended into ethanol (50 ml). To the reaction mixture was added the suspension of sodium sulfide (5 g) and sulfur (0.65 g) in ethanol (12 ml). The reaction mixture was refluxed 1.5 hour and then the resultant solid was filtered and washed with hot water and ethanol. The dry solid was slurried with acetic acid (60 ml) and acetanhydridi (35 ml). To the suspension was gradually added zinc (16.6 g) and the suspension was stirred at room temperature for 15 min before filtering off. The residue was evaporated to dryness. The product was purified by column chromatography using toluene-ethyl acetate-acetic acid 8:1:1 as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318785B2
Source datasetuspto-grants-2012_11
ORD IDord-e2b8445e6e684076841356a2e6169893
Source noteuspto-grants-2012_11