HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241966Generated: October 29, 2026
Tert-butyl 4-chloro-3-nitrobenzoate → Tert-butyl 4-(ethylamino)-3-nitrobenzoate
https://huagongshe.com/reaction/1241966
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-butyl 4-chloro-3-nitrobenzoate | HCID 10611184 | — |
| Reactant | Ethylamine tetrahydrofuran | HCID 66726184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(ethylamino)-3-nitrobenzoate | HCID 20626666 | 100.4% |
Reaction Steps
4-Chloro-3-nitrobenzoic acid tert-butyl ester (3.0 g, 11.6 mmol), prepared according to a published procedure [WO 9707101], was cautiously added to a solution of 2.0 M EtNH2/THF (20 mL, 40 mmol) and TEA (2.0 mL, 14 mmol) in anhydrous THF (30 mL). The resulting mixture was heated at 65° C. for 3 h, cooled, concentrated under reduced pressure, diluted with DCM (200 mL), washed with water (2×100 mL) and brine (50 mL), dried over anhydrous Na2SO4 and concentrated to give the title compound (3.1 g, 99%) as a yellow solid, which was used without further purification. 1H-NMR (CDCl3): δ 8.80 (1H, d), 8.24 (1H, br s), 8.02 (1H, dd), 6.84 (1H, d), 3.41 (2H, m), 1.59 (9H, s), 1.40 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115640B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4d9f744c303c4972beaa8673c09d0d6d |
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| Source note | uspto-grants-2006_10 |
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