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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350454Generated: November 2, 2026

Ethanol → HCID 23512429, compound

https://huagongshe.com/reaction/350454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantStannous ChlorideHCID 24479—
ReactantHCID 58785152HCID 58785152—
ProductHCID 23512429HCID 2351242938%

Reaction Steps

To a stirred solution of ethyl 2,3-difluoro-4-nitrophenylacetate (5.85 g, 23.9 mol) in EtOH (100 mL), was added SnCl2 (16.1 g, 71.6 mmol) at rt. The stirring was continued for 18 hours at reflux. After removal of the solvent, the residue was dissolved in CHCl3 (100 mL) and poured into ice water-4M NaOH (40 mL of 4M NaOH in 300 mL of ice-water), extracted with CHCl3 (100 mL×2), dried over anhydrous MgSO4, and concentrated under a reduced pressure. The residue was chromatographed on silica gel (middle pressure chromatography system YAMAZEN YFLC-5404, linear gradient of hexane-EtOAc from 9:1 to 7:3, φ50 mg×500 mg, 15 ml/min) to give ethyl 4-amino-2,3-difluorophenylacetic acid (1.94 g, 38%) as a colorless oil. 1H-NMR (CDCl3) δ 1.25 (t, J=7.3 Hz, 3 H), 3.55 (d, J=1.0 Hz, 2 H), 3.78 (br s, 2 H), 4.15 (dd, J=7.2 Hz, 14.2 Hz, 2 H), 6.49 (dt, J=1.8, 8.2 Hz, 1 H), 6.78 (m, 1 H); MS (FAB) m/z 216 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-50d426bc5f34447d9f49668690afdfb0
Source noteuspto-grants-2007_02