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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460369Generated: October 29, 2026

3,4,5-Triethoxyaniline → 3,5-Dimethoxy-4-methylaniline

https://huagongshe.com/reaction/460369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TriethoxyanilineHCID 18630560—
Reactant3,4,5-Triethoxy-1-iodobenzeneHCID 22933075—
Product3,5-Dimethoxy-4-methylanilineHCID 12752288—

Reaction Steps

Following the procedure of the synthesis of 3,4,5-triethoxy-1-iodobenzene from the oil containing 3,4,5-triethoxyaniline in Reference Example 5,1-iodo-3,5-dimethoxy-4-methylbenzene was obtained as a pale yellow amorphous powder (7.59 g, yield: 87%) from 3,5-dimethoxy-4-methylaniline (J. Chem. Soc., 497–506 (1963)) (5.23 g, 31.3 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196101B2
Source datasetuspto-grants-2007_03
ORD IDord-56d2c1c1760c4586a9eee957de8d7613
Source noteuspto-grants-2007_03