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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599098Generated: October 26, 2026

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

https://huagongshe.com/reaction/1599098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-nitrobenzoateHCID 1196136963.5%

Reaction Steps

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739129
Source datasetuspto-grants-1998_04
ORD IDord-3ba72393137a4e0d8e5cddb209939684
Source noteuspto-grants-1998_04