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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906157Generated: October 26, 2026

Phenol → 4-(Aminocarbonyl)-2-methyl-5-(methyloxy)benzoic acid

https://huagongshe.com/reaction/906157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantMethyl iodideHCID 6328—
ReactantMethyl 4-cyano-5-iodo-2-methylbenzoateHCID 67402433—
ReactantMethyl 4-cyano-5-hydroxy-2-methylbenzoateHCID 67404603—
Product4-(Aminocarbonyl)-2-methyl-5-(methyloxy)benzoic acidHCID 57748328—

Reaction Steps

Synthesized according to the method of reagent preparation 41 by replacement of step 6 with the conversion of methyl 4-cyano-5-iodo-2-methylbenzoate to methyl 4-cyano-5-hydroxy-2-methylbenzoate according to the method described in Chemical & Pharmaceutical Bulletin (2007), 55(9), 1361-1364 followed by phenol alkylation with iodomethane then proceeding with steps 7 and 8. 1H NMR (400 MHz, DMSO-d6): 7.69 (b, 1H), 7.63 (b, 2H), 7.45 (s, 1H), 3.88 (s, 3H), 2.44 (s, 3H); MS (EI) for C10H11NO4: 210 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-392191fc0e6849f796f9785962831b31
Source noteuspto-grants-2011_09