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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887655Generated: October 26, 2026

3-(2-Chloro-5-nitro-phenoxymethyl)-azetidine-1-carboxylic acid tert-butyl ester → 3-(5-Amino-2-chloro-phenoxymethyl)-azetidine-1-carboxylic Acid Tert-Butyl Ester

https://huagongshe.com/reaction/887655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Chloro-5-nitro-phenoxymethyl)-azetidine-1-carboxylic acid tert-butyl esterHCID 68532446—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventMethanol--water (1/1)HCID 22242641—
Product3-(5-Amino-2-chloro-phenoxymethyl)-azetidine-1-carboxylic Acid Tert-Butyl EsterHCID 68912931—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(2-chloro-5-nitro-phenoxymethyl)-azetidine-1-carboxylic acid tert-butyl ester (2.5 g, 7.29 mmol) in 60 mL of MeOH/H2O (1:1) and 3 mL of acetic acid (J. T. Baker) was added Zn powder (2.3 g, 36.47 mmol, Aldrich) at 0° C. The reaction mixture was stirred at 0° C. for 2 h then stirred at 10° C. for 2 h. The resulting mixture was filtered through a Celite® pad and the filtrate was concentrated in vacuo. The residue was treated with 60 mL of saturated aqueous NaHCO3 and extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine and dried with MgSO4. The resulting solution was concentrated in vacuo and the title compound was obtained by column chromatography (silica gel, EtOAc) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247430B2
Source datasetuspto-grants-2012_08
ORD IDord-ef12ecd2298b4f5792294bea1853b34b
Source noteuspto-grants-2012_08