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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977686Generated: October 30, 2026

3,4,5-Trimethoxyaniline → HCID 21995314, compound

https://huagongshe.com/reaction/1977686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxyanilineHCID 32285—
ReactantHCID 15405455HCID 15405455—
ProductHCID 21995314HCID 219953141.7%

Reaction Steps

2-Methylsulphonyl-4-phenoxypyrimidine (0.76 g, 3.04 mmol) and 3,4,5-trimethoxyaniline (0.56 g, 4.0 mmol) were heated as a melt at 140° for 2 h. On cooling the residue was partitioned between ethyl acetate (50 ml) and 2M hydrochloric acid (50 ml), and the organic layer was washed with water (50 ml), dried (MgSO4) and concentrated under reduced pressure. The residue was subjected to column chromatography [silica 20% ethyl acetate-hexane] to give the title compound (18 mg) as a white solid m.p. 149° after recrystallisation from ethyl acetate. δH (CDCl3) 8.26 (1H, d, J 5.6 Hz), 7.39 (2H, m), 7.26 (1H,m), 7.18-7.15 (2H, m), 6.73 (2H, s), 6.31 (1H, d, J 5.6 Hz), 3.77 (3H, s) and 3.64 (6H, s). MS m/z 354 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235746B1
Source datasetuspto-grants-2001_05
ORD IDord-2a6f3c3b7b804ac0b16e85457d977281
Source noteuspto-grants-2001_05