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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133761Generated: October 27, 2026

5-Amino-2-methoxybenzotrifluoride → HCID 67526880, compound

https://huagongshe.com/reaction/133761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methoxybenzotrifluorideHCID 600705—
Reactant2-Methyl-N-(3-methyl-4-nitrophenyl)oxirane-2-carboxamideHCID 71420003—
ProductHCID 67526880HCID 67526880—

Reaction Steps

2-Hydroxy-3-(4-methoxy-3-trifluoromethylphenylamino)-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide was prepared as described in Example 52 starting from 3-amino-6-methoxybenzotrifluoride and 2-methyloxirane-2-carboxylic acid (3-methyl-4-nitrophenyl)amide. The crude product was purified by flash chromatography (dichloromethane-1.5% methanol). 1H NMR (400 MHz, DMSO-d6): 1.41 (3H, s), 2.51 (3H, s), 3.12 (1H, dd, J=13.0 Hz, J=4.8 Hz), 3.45 (1H, dd, J=13.0 Hz, J=7.7 Hz), 3.71 (3H, s), 5.42 (1H, m), 6.00 (1H, s), 6.88 (1H, dd, J=8.9 Hz, J=2.7 Hz), 6.92 (1H, d, J=2.7 Hz), 6.97 (1H, d, J=8.9 Hz), 7.78 (1H, dd, J=8.9 Hz, J=2.3 Hz), 7.81 (1H, d, J=1.9 Hz), 8.00 (1H, d, J=8.9 Hz), 9.98 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390923B2
Source datasetuspto-grants-2008_06
ORD IDord-2000affbaedb4ed89a28ec8e63cf7150
Source noteuspto-grants-2008_06