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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386402Generated: October 29, 2026

Methanol → 5-(5-Bromo-furan-2-yl)-[1,3,4]oxadiazole-2-thiol

https://huagongshe.com/reaction/386402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromofuran-2-carbohydrazideHCID 468636—
SolventWaterHCID 962—
Product5-(5-Bromo-furan-2-yl)-[1,3,4]oxadiazole-2-thiolHCID 178527941—

Reaction Steps

5-Bromo-furan-2-carboxylic acid hydrazide (20.5 g, 100 mmol) was added to a mixture of potassium hydroxide (6.2 g, 110 mmol) and methanol (125 ml). The mixture was stirred for 30 minutes at room temperature. Carbon disulfide (15.2 g, 200 mmol) was added. The mixture was stirred at reflux for 30 hours. Water (60 ml) was added and the excess of carbon disulfide and methanol was evaporated. The aqueous suspension was acidified by adding concentrated hydrochloric acid (14 ml). The product precipitated and was washed with water (20 ml), dried and evaporated. Yield 8.58 g (35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372832B2
Source datasetuspto-grants-2013_02
ORD IDord-4f18b1e964144ee0bc28831be636126e
Source noteuspto-grants-2013_02