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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868252Generated: November 1, 2026

Trifluoroacetic acid → HCID 66643062, compound

https://huagongshe.com/reaction/1868252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66643089HCID 66643089—
SolventDichloromethaneHCID 6344—
ProductHCID 66643062HCID 66643062—

Reaction Steps

To a stirred brown solution of 2-(di-tert-butoxycarbonylamino-methyl)-6-nitro-benzoic acid methyl ester (51.53 g, 126 mmol) in methylene chloride (600 mL), was added trifluoroacetic acid (18.2 mL, 245 mmol), and the mixture was stirred at room temp overnight. Sat. sodium bicarbonate (400 mL) was added to the solution, and the mixture was stirred for 10 minutes. The organic layer was separated, dried over magnesium sulfate and evaporated to give 2-(tert-butoxycarbonylamino-methyl)-6-nitro-benzoic acid methyl ester as a brown oil (41.4 g, 106% crude yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635700B2
Source datasetuspto-grants-2009_12
ORD IDord-ad37277684b241089034c0fb1da12406
Source noteuspto-grants-2009_12