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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235855Generated: October 30, 2026

Hydrogen Sulfide → 4-(Benzyloxy)-3-propylbenzenecarbothioamide

https://huagongshe.com/reaction/2235855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantDiethylamineHCID 8021—
Reactant4-(Benzyloxy)-3-propylbenzonitrileHCID 67018773—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-3-propylbenzenecarbothioamideHCID 59300551—

Reaction Conditions

Temperature60 °C

Reaction Steps

Through a solution of 4-(benzyloxy)-3-propylbenzonitrile (1.23 g, 4.91 mmol) (Example 30) in DMF (35 mL) was passed H2S for 30 min at rt. Diethyl amine (0.76 mL, 7.36 mmol) was added and the solution was heated to 60° C. for 4 h. The mixture was cooled to rt, and the residual H2S was removed by passing argon through the solution for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was filtered through a plug of silica and washed with EtOAc. Concentration of the filtrate under reduced pressure resulted in a yellow solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714004B2
Source datasetuspto-grants-2010_05
ORD IDord-a21208bbf0ea4501a5c1d04e43987a03
Source noteuspto-grants-2010_05