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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822172Generated: October 31, 2026

3-Chloro-4-fluoroaniline → methyl N-(3-chloro-4-fluorophenyl)alaninate

https://huagongshe.com/reaction/1822172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-fluoroanilineHCID 9708—
ReactantMethyl pyruvateHCID 11748—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Productmethyl N-(3-chloro-4-fluorophenyl)alaninateHCID 54503916—

Reaction Steps

Methyl pyruvate (1-1, 42.082 g, 412.201 mmol) and 3-chloro-4-fluoroaniline (1-2, 15.000 g, 103.50 mmol) were combined in a dry pressure tube, and dissolved in cyclohexanes (400 mL). The resulting solution was treated with 10% palladium on activated carbon (7.500 g), and reacted under high pressure hydrogen gas (50 bar) for 24 h. Upon completion, the reaction mixture was filtered through celite and washed 5 times with 40 mL portions of cyclohexanes. The filtrate was concentrated under vacuum. The crude residue was purified by flash column chromotography (SiO2, 0-100% EtOAc/hexanes gradient) to give methyl N-(3-chloro-4-fluorophenyl)alaninate (1-3). 1H NMR (300 MHz, CDCl3) δ 6.94 (dd, J=8.8, 8.8 Hz, 1H), 6.60 (dd, J=6.0, 3.0 Hz, 1H), 6.42 (dd, 8.8, 6.7, 3.0 Hz 1H), 4.13 (q, J=7.0 Hz, 1H), 3.75 (m, 3H), 1.47 (d, J=6.7 Hz, 3H). MS 332.2 found, 332.6 (M+H+) required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608739B2
Source datasetuspto-grants-2009_10
ORD IDord-371a5d51ee0e4592b08391f0a4acba4f
Source noteuspto-grants-2009_10