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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441765Generated: October 30, 2026

Thionyl Chloride → 5-(Aminosulphonyl)-2-methoxybenzoyl chloride

https://huagongshe.com/reaction/441765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methoxy-5-sulfamoylbenzoic acidHCID 89601—
SolventTetrahydrofuranHCID 8028—
Product5-(Aminosulphonyl)-2-methoxybenzoyl chlorideHCID 104228—

Reaction Steps

To a suspension of the so-obtained 2-methoxy-5-sulfamoyl benzoic acid in 600 parts of anhydrous tetrahydrofuran, there were added rapidly 27.5 parts of thionyl chloride. The mixture was refluxed for 2 hours. The solution was then evaporated under vacuo. The residue was treated with 500 parts of anhydrous benzene. After elimination of benzene in vacuo, there were obtained 29 parts of 2-methoxy-5-sulfamoyl benzoyl chloride, M.P. 148°-150° C., which after one recrystallization from benzene melts at 156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04042598
Source datasetuspto-grants-1977_08
ORD IDord-42493323a870418c8c540c0c2eda2885
Source noteuspto-grants-1977_08