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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917818Generated: October 30, 2026

Sodium Dithionite → Methyl 2-amino-5-(benzyloxy)-4-methoxybenzoate

https://huagongshe.com/reaction/1917818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantMethyl 5-Benzyloxy-4-methoxy-2-nitrobenzoateHCID 22667156—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 2-amino-5-(benzyloxy)-4-methoxybenzoateHCID 22667093—

Reaction Steps

To a solution of methyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate (13.48 g, 0.0425 mol) in MeOH (700 mL) at 55° C., a concentrated solution of Na2S2O4 in water was added slowly until no more starting material was observed on TLC. The heterogeneous solution was concentrated under vacuum. The residue was treated with water (100 ml) and the mixture extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with water and brine. After drying over MgSO4, the solvent was evaporated and the residue was purified on silica gel column, using ethyl acetate/DCM (1/9) as eluent to yield methyl 2-amino-5-(benzyloxy)-4-methoxybenzoate. Yield: 7.36 g (60%). 1HNMR (DMSO-d6): δ 7.34 (5H, m), 7.25 (1H, s), 6.48 (2H, s), 6.39 (1H, s), 4.91 (2H, s), 3.80 (3H, s), 3.73 (3H, s). LC-MS (ESI) m/z 288 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-8839505dd9f548ec81742df3191259ad
Source noteuspto-grants-2013_12