Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348796Generated: October 26, 2026

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

https://huagongshe.com/reaction/348796

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 C15H2OClNO5S m/z (M+H)+=362.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-7c1e868d36bd4791a0d9f46ba899644a
Source noteuspto-grants-2007_02