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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 252218Erstellt: 25. Oktober 2026

Ammonia → Tert-butyl 3-sulfamoylbenzoate

https://huagongshe.com/reaction/252218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSulfuric AcidHCID 1118—
Edukttert-ButanolHCID 6386—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktBenzoic acid, 3-(chlorosulfonyl)-HCID 77641—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 3-sulfamoylbenzoateHCID 5973369542,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Sulfuric acid (conc., 498 μL, 9.06 mmol) was added to a suspension of MgSO4 (4.36 g, 36.22 mmol) in CH2Cl2 (36 mL). The reaction mixture was stirred for 15 minutes, treated with 3-chlorosulfonyl-benzoic acid (Aldrich, 2 g, 9.06 mmol) and 2-methyl-propan-2-ol (anhydrous, 4.33 mL, 45.27 mmol), capped tightly, and stirred overnight at room temperature. The next day, the mixture was cooled to 0° C., treated with 7N NH3 in methanol (Aldrich, 40 mL) dropwise, and stirred for 30 minutes. The solvents were removed in vacuo and the crude was dissolved in ethyl acetate and saturated NaHCO3. The organic layer was washed with saturated NaHCO3, water, and brine, dried over MgSO4, filtered, and concentrated in vacuo to afford the title compound as a white solid (1 g, 42.9% yield). 1H-NMR (CDCl3): δ 8.51-8.53 (m, 1H), 8.20-8.21 (m, 1H), 8.08-8.11 (m, 1H), 7.57-7.62 (m, 1H), 5.09 (bs, 2H), and 1.61 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07868023B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-5cf8e981a9a04de19c96d38c95f3a4b8
Quellennotizuspto-grants-2011_01