HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771140Generated: November 4, 2026
tert-Butyl piperazine-1-carboxylate → HCID 89838245, compound
https://huagongshe.com/reaction/1771140
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Tert-butyl-4-methoxybenzaldehyde | HCID 3774604 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89838245 | HCID 89838245 | — |
Reaction Steps
The synthesis is carried out in argon condition. 2 g (10.7 mmol) of N-Boc-piperazine and 2.06 g (10.7 mmol) of 3-tert-butyl-4-methoxybenzaldehyde are mixed in 30 ml of dry dichloromethane. After dissolution 2 drops of acetic acid is added, then 4.24 g (20 mmol) of NaBH(OAc)3 is added and the mixture is stirred for 12 h at 20° C. Then 20 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 (3.5 g of yellow oil) is used on the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09249115B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-ca309766a7ba40cb872c77b83d3d0e2f |
|---|
| Source note | uspto-grants-2016_02 |
|---|