HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11808Generated: October 29, 2026
Water → (R)-4-carbobenzyloxy-1-(4,5-dichloro-2-nitrophenyl)-piperazine-2-carboxylic acid
https://huagongshe.com/reaction/11808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (R)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acid | HCID 1514272 | — |
| Reactant | HCID 21976691 | HCID 21976691 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (R)-4-carbobenzyloxy-1-(4,5-dichloro-2-nitrophenyl)-piperazine-2-carboxylic acid | HCID 11487840 | 94.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098338B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-c3f0ffdbe3a147e5b8c4869da58c2e70 |
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| Source note | uspto-grants-2006_08 |
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