Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388201Generated: November 2, 2026

Carbon Dioxide → HCID 70598027, compound

https://huagongshe.com/reaction/1388201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTert-ButylamineHCID 6385—
Reactant2-MethylthiopheneHCID 11126—
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant3-Ethyl-2-methylthiopheneHCID 6427111—
ReactantHCID 23331879HCID 23331879—
ReactantButyllithiumHCID 178418339—
ProductHCID 70598027HCID 70598027—

Reaction Steps

3-ethyl-2-methyl-thiophene [W. Steinkopf, A. Merckoll and H. Straunch, Liebigs Ann. Chem. 545,45 (1940)] was reacted, analogous to 2-methyl-thiophene (see Example 5) with phosphorus pentachloride and chlorosulfonic acid, and the resulting sulfochloride was treated with tert. butylamine. By metalizing with n-butyl-lithium and carboxylating with carbon dioxide, also in analogy to the preparation of 5-methyl-2-(N-tert. butyl) sulfamoyl-thiophene-3-carboxylic acid, 4-ethyl-5-methyl-2-(N-tert. butyl) sulfamoyl-thiophene-3-carboxylic acid was obtained. Rf -value: 0.27 (TLC-prefabricated plates, silica gel 60 F254, thickness of the layer 0.25 mm, eluant:ethylene chloride/ethyl acetate/glacial acetic acid 100:30:5);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04430355
Source datasetuspto-grants-1984_02
ORD IDord-9b4e6daf445d44f9b1660d14970d70b6
Source noteuspto-grants-1984_02