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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061206Generated: November 2, 2026

Benzoic acid 4-benzyloxy-3-nitro-phenyl ester → Benzoic acid 3-amino-4-benzyloxy-phenyl ester

https://huagongshe.com/reaction/1061206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid 4-benzyloxy-3-nitro-phenyl esterHCID 53642911—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid 3-amino-4-benzyloxy-phenyl esterHCID 8658454279.3%

Reaction Steps

A Parr hydrogenator was charged with platinum(IV) oxide(PtO2) (0.3 g) and a solution of benzoic acid 4-benzyloxy-3-nitro-phenyl ester (5.23 g, 15 mmol) (which was obtained in Example 15) in methanol (80 mL) and CH2Cl2(40 mL). This mixture was then hydrogenated at 5 psi of hydrogen at 0˜10° C. for 2 hours. The reaction mixture was filtered through a short pad of celite and concentrated. Recrystallization from CH2Cl2/hexanes gave the title compound as a white solid (3.80 g, 79%); 1H NMR (300 MHz, CDCl3) δ 5.09 (s, 2H), 6.57 (dd, J=10.1, 2.7 Hz, 1H), 7.10 (d, J=2.7 Hz, 1H), 7.30-7.50 (m, 8H), 7.55-7.65 (m, 1H), 8.15-8.25 (m, 2H); MS (ES) m/z: 320.0 (MH+, 100%); HRMS Calcd. for C20H18NO3 (MH+): 320.1281. Found: 320.1278.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-5c77ab50f1064855937c1a5cf0f4b548
Source noteuspto-grants-2003_02