HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482340Generated: October 25, 2026
Benzoyl chloride, 3-nitro- → Tert-butyl 3-nitrobenzoate
https://huagongshe.com/reaction/482340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-nitrobenzoate | HCID 11961369 | 63.5% |
Reaction Steps
Potassium t-butoxide (3.82 g, 32.30 mmol) is added to a solution of 3-nitrobenzoyl chloride (5.00 g, 26.94 mmol) in anhydrous THF (70 mL) and stirred under nitrogen for 2 hrs. The reaction mixture is concentrated in vacuo and partitioned between DCM and water. After separating the phases, the aqueous layer is back-extracted with ethyl acetate. The organic layers are combined, dried over anhydrous magnesium sulfate, filtered and then concentrated in vacuo. The crude product is purified on flash grade silica gel using 0-5% gradient of ethyl acetate in n-hexane. Fractions containing the product are combined, concentrated in vacuo, and then dried under high vacuum to provide the title compound as an oil (3.82 g, 17.1 mmol). 1H NMR (300 MHz, CDCl3) δ=1.63 (s, 9H); 7.62 (t, J=7.9 Hz, 1H); 8.29-8.41 (m, 2H); 8.78-8.80 (m, 1H). MS (Cl): [M+H]+ =224.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05795887 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-be1c5ba31c0b42b58399cd0d291adb63 |
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| Source note | uspto-grants-1998_08 |
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