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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509509Generated: October 30, 2026

Trifluoroacetic acid → HCID 68730762, compound

https://huagongshe.com/reaction/509509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68729664HCID 68729664—
SolventDichloromethaneHCID 6344—
ProductHCID 68730762HCID 68730762—

Reaction Steps

To a stirred brown solution of 4-(di-tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid methyl ester (95.97 g, 233.8 mmol) in methylene chloride (800 mL), was added trifluoroacetic acid (33.87 mL, 455.9 mmol), and the mixture was stirred at room temperature overnight. Sat. sodium bicarbonate (500 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 4-(tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid methyl ester as a brown oil (64.36 g, 88% crude yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096573B2
Source datasetuspto-grants-2015_08
ORD IDord-f65963379fbe45c5866cae57add6e014
Source noteuspto-grants-2015_08