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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-4-fluorobenzoateHCID 12541234—
Reactant2-(Tert-butoxy)ethanamineHCID 21914614—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-N-(2-tert-butoxyethyl)-4-fluorobenzamideHCID 86695682—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883819B2
Source datasetuspto-grants-2014_11
ORD IDord-d08b0bf3bb674261909543edc893948b
Source noteuspto-grants-2014_11