HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549656Generated: October 28, 2026
Benzyl chloroformate → 1,4-Bis(benzyloxycarbonyl)piperazine-2-carboxylic acid
https://huagongshe.com/reaction/549656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Piperazine-2-carboxylic acid dihydrochloride | HCID 2723757 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,4-Bis(benzyloxycarbonyl)piperazine-2-carboxylic acid | HCID 22632859 | 96% |
Reaction Steps
Piperazine-2-carboxylic acid dihydrochloride (10.0 g, 49.2 mmol) was dissolved in H2O (125 mL) and 1,4-dioxane (200 mL), and the solution was brought to pH 11 with 50% NaOH in H2O. Benzyl chloroformate (14 mL, 98 mmol) was added while maintaining the pH at 11 with 50% NaOH in H2O. After 1 h, an additional portion of benzyl chloroformate (2 mL, 14 mmol) was added. After 30 min, the solution was extracted with Et2O (3×100 mL). The aqueous layer was brought to pH 2 with concentrated HCl and extracted with EtOAc (3×200 mL). The combined EtOAc extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure to give 18.9 g (96%) of the desired product as a thick oil. The material was used without further purification. LC-MS: RT=9.250 min; [M+H]+=421.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943622B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-56d8a80f3e694a888fbc6e8a4e9a60ef |
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| Source note | uspto-grants-2011_05 |
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