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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566062Generated: October 26, 2026

4-Nitrobenzaldehyde → HCID 18472662, compound

https://huagongshe.com/reaction/566062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantGlycine, N-methyl-, methyl ester, hydrochloride (1:1)HCID 83544—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 18472662HCID 1847266280.2%

Reaction Steps

In 1,2-dichloroethane (50 ml) were suspended p-nitrobenzaldehyde (5 g), sarcosine methyl ester hydrochloride (4.6 g) and triethylamine (4.6 ml), and to the mixture was added, under ice-cooling, triacetoxy sodium boron hydride (9.8 g). Under nitrogen atmosphere, the mixture was stirred at room temperature for 4 hours. To the mixture was added water, and the mixture was concentrated, neutralized with sodium hydroxide solution and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column (ethyl acetate/hexane) to give N-(4-nitrobenzyl)sarcosine methyl ester (6.3 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-ec5112c45ac9435d8695ad166943129b
Source noteuspto-grants-2001_01