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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990833Generated: October 25, 2026

(3-Amino-5-ethoxy-4-iodo-phenyl)-methanol → 3-Amino-5-ethoxy-4-iodo-benzaldehyde

https://huagongshe.com/reaction/1990833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Amino-5-ethoxy-4-iodo-phenyl)-methanolHCID 68454929—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3-Amino-5-ethoxy-4-iodo-benzaldehydeHCID 5870635364.5%

Reaction Steps

To a solution of (3-amino-5-ethoxy-4-iodo-phenyl)-methanol (4.9 g, 16.72 mmol, 1.0 equiv) in dichloromethane (100 mL) was added activated MnO2 (7.27 g, 83.59 mmol, 5.0 equiv) and the reaction mixture heated to reflux for 3 h. Filtration through Hyflo Super Cel, concentration by evaporation under reduced pressure and purification with column chromatography on silica eluting with hexane/ethyl acetate (3:1) yielded 3.14 g (60%) of the title compound. 1H NMR (300 MHz, DMSO): δ 1.37 (t, J=7.0 Hz, 3H), 4.15 (q, J=7.0 Hz, 2H), 4.49 (d, J=5.6 Hz, 2H), 5.21 (t, J=5.6 Hz, 1H), 6.82 (s, 1H), 6.85 (s, 1H), 11.64 (br s, 1H). 13C NMR (75 MHz, DMSO): δ 14.61, 62.89, 64.26, 100.74, 106.46, 117.80, 137.50, 142.74, 144.05, 154.54. MS (ISP): 291.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-e88486c99e6e4cf5b4a4565d32a444ad
Source noteuspto-grants-2010_01