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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867246Generated: October 31, 2026

Trifluoroacetic acid → HCID 57979480, compound

https://huagongshe.com/reaction/1867246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-Nitrophthalic acidHCID 69043—
Reactant2-Amino-6-(methoxycarbonyl)benzoic acidHCID 13659967—
SolventMethanolHCID 887—
ProductHCID 57979480HCID 57979480—

Reaction Steps

2-Amino-6-(methoxycarbonyl) benzoic acid (1) was made from 3-nitrophthalic acid using the procedure first reported by Rogers and Averill (Rodgers, M. E. and Averill, B. A., J. Org. Chem., 1986, 51, 3308) and then used immediately to make Diels Alder cycloadduct 2 via the 3-(methoxhycarbonyl)dehydrobenzene intermediate that is generated under aprotic diazotization reaction conditions (based on modified conditions first reported by Giles, R. G. F., Sargent, M. V., and Sianipar, H., J. Chem. Soc. Perkin Trans I, 1991, 1571). Treatment of cycloadduct 2 with TFA in refluxing methanol yielded a 1:2 mixture of regioisomeric naphthols 3a and 3b which were separated by column chromatography on silica gel. The 1,5-naphthol regioisomer (3a) was then reduced with LAH to produce 5-hydroxymethyl naphthol 4, which was then coupled to carbapenem intermediate 5 (CPI 5) with catalytic palladium to produce the 1-carbon naphthol coupled CPI 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632828B2
Source datasetuspto-grants-2009_12
ORD IDord-f6e39f17ecc54888833ea29b15f2d875
Source noteuspto-grants-2009_12