HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771139Generated: October 30, 2026
tert-Butyl piperazine-1-carboxylate → HCID 89838520, compound
https://huagongshe.com/reaction/1771139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Benzaldehyde, 2,3,4-triethoxy- | HCID 19956854 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89838520 | HCID 89838520 | — |
Reaction Steps
The synthesis is carried out in argon condition. 1.1 g (5.9 mmol) of N-Boc-piperazine and 1.40 g (5.9 mmol) of 2,3,4-triethoxybenzaldehyde are mixed in 25 ml of dry dichloromethane. After dissolution 2 drops of acetic acid is added, then 2.12 g (10 mmol) of NaBH(OAc)3 is added and the mixture is stirred for 12 h at 20° C. Then 10 ml of 5% NaHCO3 aqueous solution is added dropwise with care to the reaction mixture. The organic layer is separated, washed with 5% Na2CO3 solution, dried over sodium sulfate, filtered off and concentrated in vacuum at 50÷80° C. The residue (2.2 g of yellowish oil) is used on the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249115B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-d62b6eb34aa44fea8b6513ab94e67292 |
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| Source note | uspto-grants-2016_02 |
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