HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335316Generated: October 27, 2026
Methyl 3-amino-4-fluorobenzoate → 3-Amino-N-(2-tert-butoxyethyl)-4-fluorobenzamide
https://huagongshe.com/reaction/335316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3-amino-4-fluorobenzoate | HCID 12541234 | — |
| Reactant | 2-(Tert-butoxy)ethanamine | HCID 21914614 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-N-(2-tert-butoxyethyl)-4-fluorobenzamide | HCID 86695682 | — |
Reaction Steps
A mixture comprising 2-tert-butoxyethanamine (1.2 g, 5.12 mmol, 50% w/w) and methyl 3-amino-4-fluorobenzoate (0.866 g, 5.12 mmol) in THF (10 ml) was treated with TBD (0.713 g, 5.12 mmol) and heated at 90° C. for 16 hrs. After cooling to RT, the solvent was removed in vacuo and the residue was partitioned between water and EtOAc. The organic portion was separated and washed with 10% aq citric acid (×2), NaHCO3 (sat. aq), brine, dried (MgSO4) and concentrated in vacuo. Purification of the crude product by chromatography on silica eluting with 0-100% EtOAc in iso-hexane afforded the title compound as a clear oil;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883819B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d08b0bf3bb674261909543edc893948b |
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| Source note | uspto-grants-2014_11 |
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