Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915403Generated: October 31, 2026

Hydrochloric Acid → 2-Tert-butyl-5-nitrobenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1915403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium SulfiteHCID 24437—
Reactant2-Tert-butyl-5-nitroanilineHCID 826103—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product2-Tert-butyl-5-nitrobenzene-1-sulfonyl chlorideHCID 5747026417%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

A suspension of 2-tert-butyl-5-nitrobenzenamine (0.971 g, 5 mmol) in conc. HCl (5 mL) was cooled to 5-10° C. and a solution of NaNO2 (0.433 g, 6.3 mmol) in H2O (0.83 mL) was added dropwise. Stirring was continued for 0.5 h, after which the mixture was vacuum filtered. The filtrate was added, simultaneously with a solution of Na2SO3 (1.57 g, 12.4 mmol) in H2O (2.7 mL), to a stirred solution of CuSO4 (0.190 g, 0.76 mmol) and Na2SO3 (1.57 g, 12.4 mmol) in HCl (11.7 mL) and H2O (2.7 mL) at 3-5° C. Stirring was continued for 0.5 h and the resulting precipitate was filtered off, washed with water and dried to give 2-tert-butyl-5-nitrobenzene-1-sulfonyl chloride (0.235 g, 17%). 1H NMR (400 MHz, DMSO-d6) δ 9.13 (d, J=2.5 Hz, 1H), 8.36 (dd, J=8.9, 2.5 Hz, 1H), 7.88 (d, J=8.9 Hz, 1H), 1.59 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614327B2
Source datasetuspto-grants-2013_12
ORD IDord-ddba171cac2b4c758d5cb276b663cbc3
Source noteuspto-grants-2013_12