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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242280Generated: October 30, 2026

2-(3-Methoxy-propyl)-4-nitro-phenoxy-acetic acid ethyl ester → 4-Amino-2-(3-methoxy-propyl)-phenoxy-acetic acid ethyl ester

https://huagongshe.com/reaction/1242280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Methoxy-propyl)-4-nitro-phenoxy-acetic acid ethyl esterHCID 67072433—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Amino-2-(3-methoxy-propyl)-phenoxy-acetic acid ethyl esterHCID 67072087—

Reaction Steps

3.00 g (roughly 65%, 6.56 mmol) of the above prepared [2-(3-methoxy-propyl)-4-nitro-phenoxy]-acetic acid ethyl ester was hydrogenated at RT in 50 ml of AcOEt over 0.60 g of Pd/C (10%) under 1 atm of H2-pressure. After 3 h at ambient temperature, the reaction mixture was filtered over Celite and carefully rinsed with AcOEt. Evaporation of the solvent, followed by flash chromatography (SiO2, hexane/AcOEt=1/1) produced 1.69 g of the title compound as light brown oil; from the more polar fractions, 0.784 g of 8-(3-methoxy-propyl)-4H-benzo[1,4]oxazin-3-one was isolated (cyclized reduced ortho-amino derivative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-eeb36b2553e64da4a0538fb01f09499d
Source noteuspto-grants-2006_10