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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266491Generated: October 25, 2026

Ethanethiol → HCID 67596278, compound

https://huagongshe.com/reaction/266491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant2-(1-Phenyltetrazol-5-yl)thiomethyl-4-isopropyl-5,6-dimethoxy-saccharinHCID 44341378—
SolventChloroformHCID 6212—
ProductHCID 67596278HCID 6759627877%

Reaction Steps

2-(1-phenyltetrazol-5-yl)thiomethyl-4-isopropyl-5,6-dimethoxy-saccharin (0.48 g) was added with stirring at 0° C. to a solution of aluminum chloride (0.4 g) and ethanethiol (0.15 mL) in chloroform (3 mL). The temperature was allowed to rise to and remain at room temperature for 18 hours. The reaction mixture was passed through silica gel with ethyl acetate-hexane (2:3) as eluant affording as a colorless oil 2-(1-phenyltetrazol-5-yl)thiomethyl-4-isopropyl-5-hydroxy-6-methoxy-saccharin, 0.3 g, 77% yield, whose structure was proven by proton and carbon-13 magnetic resonance, mass spectrometric and nuclear Overhauser enhancement analyses. The latter analysis showed 19% enhancement of the methoxy protons signal and 10% enhancement of the C-7 proton signal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-ae3e2977941043129530b19f70808fec
Source noteuspto-grants-1997_07