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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46666Generated: November 3, 2026

Hydrogen Sulfide → HCID 20386623, compound

https://huagongshe.com/reaction/46666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 20386683HCID 20386683—
SolventEthanolHCID 702—
SolventO-XyleneHCID 7237—
ProductHCID 20386623HCID 2038662361.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a 1-l stainless steel autoclave were placed 56.2 g (0.150 mole) of 1,2-diphenyl-4-(2,4-dimethoxyphenyl)butane-1,4-dione, 100 ml of xylene, 33.3 g (0.075 mole) of phosphorus pentasulfide and 120 g of hydrogen sulfide. The contents of the autoclave were stirred at 160°-162° C. (1040-1080 psig) for three hours. The autoclave was then cooled, and the remaining hydrogen sulfide was vented into a trap of aqueous sodium hydroxide. The residue was stirred with 150 ml of absolute ethanol to destroy excess phosphorus pentasulfide. Chilling to -78° C. and filtration gave 27.6 g (49.4%) of crude product, m.p. 107°-110° C. Recrystallization from 30 ml of dioxane and 60 mll of ethanol gave 17.3 g (31%) of pure 2,3-diphenyl-5-(2,4-dimethoxyphenyl)thiophene, m.p. 112°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-dab0657f93fa4b42ba3a1fe5153c2d75
Source noteuspto-grants-1979_11