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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841949Generated: October 29, 2026

Water → (R)-4-carbobenzyloxy-1-(4,5-dichloro-2-nitrophenyl)-piperazine-2-carboxylic acid

https://huagongshe.com/reaction/841949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant(R)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acidHCID 1514272—
ReactantHCID 21976691HCID 21976691—
SolventTriethylamineHCID 8471—
Product(R)-4-carbobenzyloxy-1-(4,5-dichloro-2-nitrophenyl)-piperazine-2-carboxylic acidHCID 1148784094.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a slurry containing 5.0 g of (R)-4-carbobenzyloxypiperazine-2-carboxylic acid, 4.2 g of 1,2-dichloro-fluoro-5-nitrobenzene, 85 mL of water and 170 mL of dimethylformamide is added slowly 5.3 mL of triethylamine. The solution is heated to 50° C. for 5 hours, then at ambient temperature overnight. The dark orange solution is concentrated under reduced pressure (1-2 mm, <50° C.) to an orange oily residue. This oil is dissolved in 400 mL of ethyl acetate and washed with 100 mL of 1 N HCl (2×), with 150 mL of water (2×), and 100 mL of brine. The organic layer is dried over MgSO4, filtered and concentrated to give 8.1 g (94.2%) of title compound as an orange solid foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372745B1
Source datasetuspto-grants-2002_04
ORD IDord-466533a296c0430e9affcc39d80fee71
Source noteuspto-grants-2002_04