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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1599098Erstellt: 27. Oktober 2026

Benzoyl chloride, 3-nitro- → Tert-butyl 3-nitrobenzoate

https://huagongshe.com/reaction/1599098

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chloride, 3-nitro-HCID 8495—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 3-nitrobenzoateHCID 1196136963,5%

Reaktionsschritte

Potassium t-butoxide solid (3.82 g, 32.30 mmol) was added to a solution of 3-nitrobenzoyl chloride (5.00 g, 26.94 mmol) in dry tetrahydrofuran (70 mL) and stirred under nitrogen for 2 hrs. The reaction mixture was concentrated in vacuo and partitioned between dichloromethane and water. After separating the phases, the aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, dried over anhydrous magnesium sulfate, filtered and then concentrated in vacuo. The crude product was purified on flash grade silica gel using 0-5% gradient of ethyl acetate in n-hexane. Fractions containing the product were combined, concentrated in vacuo, and then dried under high vacuum to provide 3.82 g of the title compound as an oil. 1H NMR (300 MHz, CDCl3) d 8.79 (m, 1H), 8.35 (m, 2H), 7.62 (m, 1H), 1.63 (s, 9H); low resolution MS (Cl) m/e 224 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05739129
Quelldatensatzuspto-grants-1998_04
ORD IDord-3ba72393137a4e0d8e5cddb209939684
Quellennotizuspto-grants-1998_04