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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086743Generated: October 27, 2026

Hydrochloric Acid → Methyl 2-(chlorosulfonyl)-6-fluorobenzoate

https://huagongshe.com/reaction/1086743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantChlorineHCID 24526—
ReactantMethyl 2-amino-6-fluorobenzoateHCID 2818492—
ReactantSodium NitriteHCID 23668193—
CatalystCupric ChlorideHCID 24014—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductMethyl 2-(chlorosulfonyl)-6-fluorobenzoateHCID 14257491—

Reaction Conditions

Temperature5 °C

Reaction Steps

At 5° C. and while stirring, 108 g (0.64 mol) of methyl 6-fluoroanthranilate and 45 g (0.65 mol) of sodium nitrite in 106 ml of water were added separately but simultaneously over a period of 1 hour in such a manner to 250 ml of concentrated hydrochloric acid that the ester component was in an excess. After the reaction mixture had been stirred for 20 minutes at 5 to 8° C., it was poured all at once into a prepared solution of 53 g of sulfur dioxide, 1.7 g of copper (II) chloride in a small amount of water and 200 ml of 1,2-dichloroethane, and stirred for a further 10 minutes. The mixture was heated slowly to 50° C. and stirred for ninety minutes while passing in 46 g of sulfur dioxide. The mixture was then cooled to 20° C. and 5.5 g of chlorine was passed in over a 20-minute period while stirring. The organic phase was then separated, washed with water and dried. There was obtained 65% of theory of the title compound as a brownish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032167
Source datasetuspto-grants-1991_07
ORD IDord-9031adb024a74cd8be24ca32b5eeb96e
Source noteuspto-grants-1991_07