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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364309Generated: October 31, 2026

Sulfur Dioxide → Methyl 2-chloro-5-sulfamoylbenzoate

https://huagongshe.com/reaction/1364309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
ProductMethyl 2-chloro-5-sulfamoylbenzoateHCID 13960349—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To methyl 5-amino-2-chlorobenzoate (16.2 g) in concentrated hydrochloric acid (40 ml)/acetic acid (120 ml) suspension, a sodium nitrite (7.6 g) aqueous solution (20 ml) was added under ice cooling and the mixture was stirred at that temperature for 45 minutes. Next, the inside temperature of the reaction vessel was cooled to −5° C., copper (II) chloride 2-hydrate (3.7 g) and a 21% sulfur dioxide in acetic acid solution (60 ml) were added, and the mixture was raised to room temperature and stirred at 12 hours. Under ice cooling, distilled water was added to the reaction solution, the mixture was stirred at that temperature for 30 minutes, and the precipitate was collected by filtration. The filtrate was dissolved in tetrahydrofuran (50 ml), 28% ammonia water (10 ml) was added under ice cooling, and the mixture was stirred at that temperature for 15 minutes. The tetrahydrofuran was distilled off in vacuo, then ethyl acetate/hexane was added. The precipitate was collected by filtration to obtain the title compound (10.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888348B2
Source datasetuspto-grants-2011_02
ORD IDord-aa4c07bf4c0b41df8e2df69fb1f791bd
Source noteuspto-grants-2011_02