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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987740Generated: November 1, 2026

Hydrochloric Acid → Methyl 3-(chlorosulfonyl)-5-[(dipropylamino)carbonyl]-Benzoate

https://huagongshe.com/reaction/1987740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantMethyl 3-amino-5-[(dipropylamino)carbonyl]BenzoateHCID 22593627—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 3-(chlorosulfonyl)-5-[(dipropylamino)carbonyl]-BenzoateHCID 22593631—

Reaction Steps

Methyl 3-amino-5-[(dipropylamino)carbonyl]benzoate (XXXI, PREPARATION 10, 1.11 g, 4 mmol) is added to a mixture of water (5 mL) and concentrated hydrochloric acid (1 mL). Sodium nitrite (0.276 g, 4 mmol) is added to the mixture slowly at 0 degrees C. The mixture is then added to an acetic acid solution (5 mL) of CuCl2.2H2O saturated with sulfur dioxide. The mixture is stirred for 0.5 hours and poured into ice water. The mixture is extracted with ethyl acetate. The organic phase is separated and washed with saturated sodium bicarbonate, water, and saline and dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound, NMR (300 MHz, CDCl3) delta 8.69, 8.38, 8.20, 4.01, 3.49, 3.14, 1.72, 1.59, 1.01 and 0.79; MS (ESI+) for C15H20ClNO5S m/z (M+H)+=362.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553831B2
Source datasetuspto-grants-2009_06
ORD IDord-a4fa37b2bb4d48eda6915cbce4744feb
Source noteuspto-grants-2009_06