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HRID 423902Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/423902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium SulfiteHCID 24437—
Edukt2-Tert-butyl-5-nitroanilineHCID 826103—
EduktSodium NitriteHCID 23668193—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelWaterHCID 962—
Produkt2-Tert-butyl-5-nitrobenzene-1-sulfonyl chlorideHCID 5747026417%

Reaktionsbedingungen

Temperatur7.5 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08101767B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-45bf0fa48e1f4e329950cab5ab128f25
Quellennotizuspto-grants-2012_01