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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372199Generated: October 26, 2026

Dimethyl Sulfoxide → 4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acid

https://huagongshe.com/reaction/372199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant4-((Benzyloxy)carbonyl)piperazine-2-carboxylic acidHCID 5058362—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acidHCID 12109643—

Reaction Steps

A mixture of 12.0 g. (0.04 mole) of 4-carbobenzoxypiperazine-2-carboxylic acid, 8.4 g. (0.06 mole) of o-nitrofluorobenzene, 16 g. of triethylamine and 100 ml. of dimethylsulfoxide is heated at 90° for 8 1/2 hours, cooled, diluted with water (300 ml.) and extracted with ether. The aqueous phase is then acidified with dilute hydrochloric acid and extracted with ether. The combined ether extracts are diluted with 1/3 its volume of pentane. The ether-pentane solution is washed with water, dried (MgSO4) and concentrated to give 14 g. of yellow-orange glassy product. Thin layer chromatrgraphy analysis (1% acetic acid in benzene on a silica gel plate) shows 1 main spot with a faint second impurity spot.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04089958
Source datasetuspto-grants-1978_05
ORD IDord-a0edf31317c248e5b4191da6c11de254
Source noteuspto-grants-1978_05