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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453017Generated: October 30, 2026

Diethyl Ether → 5-(Tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid

https://huagongshe.com/reaction/453017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 5-tert-butoxycarbonylaminomethyl-2-nitrobenzoateHCID 19698365—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(Tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acidHCID 6669714941.9%

Reaction Steps

A mixture of 5-(tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid methyl ester (52.5 g, 169.3 mmol), lithium hydroxide (4.86 g, 203.1 mmol) in methanol (546 mL) and water (273 mL) was stirred with a mechanical stirrer at room temp overnight. The methanol was evaporated, and to the aqueous solution, was added 1 N HCl (270 mL) to form the precipitate. Ether (350 mL) was added, and the mixture was stirred at 0° C. for 2 hours. The mixture was evaporated. To the residue, was added water (500 mL). The aqueous layer was extracted with methylene chloride (3×100 mL). The combined organic layers were separated, dried over magnesium sulfate, and concentrated to give 5-(tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid as a brown oil (21.0 g, 41% yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492395B2
Source datasetuspto-grants-2013_07
ORD IDord-7462abbbd46448b3b97b8e0c1a5b7531
Source noteuspto-grants-2013_07