Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223319Generated: October 27, 2026

Hydrogen Sulfide → HCID 22744791, compound

https://huagongshe.com/reaction/2223319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantEther hydrochlorideHCID 10953452—
Reactant2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-thiobenzimidic acid ethyl esterHCID 20628395—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22744791HCID 22744791—

Reaction Conditions

Temperature45 °C

Reaction Steps

As shown in Scheme 9, hydrogen sulfide gas (2 mL) was condensed into a cooled (−78° C.) solution of 2.8 grams (6.8 mmol) of 2-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-3-chloro-thiobenzimidic acid ethyl ester and 13.6 mL (13.6 mmol) of 1.0 M HCl/ether in 100 mL of tetrahydrofuran. The reaction was heated to 45° C. and stirred overnight in a sealed tube. The reaction mixture was diluted with water and extracted with methylene chloride once, organic layer was washed with brine, dried (MgSO4), filtered and evaporated to give a crude orange oil. The oil was partially purified by chromatography through a short column of silica gel (eluting with 5:95 ethyl acetate/hexanes) which resulted in 1.8 g of an orange powder which was used directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375125B2
Source datasetuspto-grants-2008_05
ORD IDord-7e7cb8d17a654d90bdcc2970412cc63e
Source noteuspto-grants-2008_05