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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279772Generated: October 30, 2026

Hydrochloric Acid → Diethyl 3-chloro-4-aminobenzylphosphonate

https://huagongshe.com/reaction/2279772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl 3-chloro-4-nitrobenzylphosphonateHCID 86654007—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductDiethyl 3-chloro-4-aminobenzylphosphonateHCID 19077629—

Reaction Steps

A solution of diethyl (3-chloro-4-nitrobenzyl)phosphonate (Compound 24E, 0.500 g, 1.62 mmol) in EtOH (10 mL) was charged with iron (0.454 g, 8.12 mmol) and heated to reflux. When the reaction mixture reached reflux, it was charged with 0.1 N aq HCl (0.500 mL, 0.08 mmol) and stirred for 10 min. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated in vacuo. The compound was purified on an Teledyne Isco Combiflash® Rf system eluting with 40 to 90% EtOAc in heptane to afford the title compound. 1H NMR (400 MHz, chloroform-d) δ 7.19 (t, J=2.40 Hz, 1H), 7.01 (td, J=2.27, 8.08 Hz, 1H), 6.71 (dd, J=0.63, 8.21 Hz, 1H), 3.96-4.08 (m, 4H), 2.96-3.06 (m, 2H), 1.26 (t, J=7.07 Hz, 6H); MS (ES+): m/z: 278.06 [MH+]. UPLC: tR=1.18 min (UPLC-TOF: polar—3 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133224B2
Source datasetuspto-grants-2015_09
ORD IDord-ae2cb123de1d40528e4a7bb4a1a92d67
Source noteuspto-grants-2015_09