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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354392Generated: November 1, 2026

Ethanol → HCID 23511851, compound

https://huagongshe.com/reaction/354392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantStannous ChlorideHCID 24479—
ReactantHCID 53419355HCID 53419355—
ProductHCID 23511851HCID 2351185152%

Reaction Steps

To a stirred solution of ethyl 2,5-difluoro-4-nitrophenylacetate (5.88 g, 25.4 mol) in EtOH (100 mL), was added SnCl2 (17.2 g, 76.3 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 mm×500 mm, 15 mm) to give ethyl 4-amino-2,5-difluorophenylacetic acid (2.85 g, 52%) as a colorless oil. 1H-NMR (CDCl3) δ1.28 (t, J=7.3 Hz; 3H), 3.51 (s, 2H), 3.78 (brs, 2H), 4.15 (dd, J=7.2 Hz, 14.2 Hz, 2H), 6.47 (dd, J=7.5, 10.4 Hz, 1H), 6.88 (dd, J=6.7, 11.0 Hz, 1H); MS (FAB) m/z 216 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-dba76dc2f69148d0a2685da8d2b474af
Source noteuspto-grants-2004_06