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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833406Generated: November 1, 2026

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

https://huagongshe.com/reaction/1833406

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 elmination 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 numberUS04066662
Source datasetuspto-grants-1978_01
ORD IDord-98f8930e9ab8424f9c168450c724ab70
Source noteuspto-grants-1978_01