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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46660Generated: October 30, 2026

Hydrogen Sulfide → 2,3-Diphenyl-5-o-chlorophenylthiophene

https://huagongshe.com/reaction/46660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 53746567HCID 53746567—
SolventO-XyleneHCID 7237—
Product2,3-Diphenyl-5-o-chlorophenylthiopheneHCID 5392582667.3%

Reaction Steps

A 1-liter stainless steel stirred autoclave was charged with 33 g. (0.0946 mole) of 1,2-diphenyl-4-o-chlorophenylbutane-1,4-dione, 100 ml. of xylene, 20 g of phosphorus pentasulfide and 125 g of hydrogen sulfide. The autoclave was then heated at 160°-187° C. for three hours. The autoclave was cooled and vented. The residue was washed with ethanol and filtered off to give 17 g (51.8%) of crude product, m.p. 103°-107° C. Recrystallization from 20 ml of dioxane and 40 ml of ethanol gave 10.5 g (32%) of pure product, m.p. 117°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174405
Source datasetuspto-grants-1979_11
ORD IDord-7753e8950ee947498c91a91e32258812
Source noteuspto-grants-1979_11