HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278201Generated: October 30, 2026
tert-Butyl piperazine-1-carboxylate → HCID 89676972, compound
https://huagongshe.com/reaction/2278201
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Chloro-6-(1-pyrrolidinyl)benzaldehyde | HCID 28603569 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 89676972 | HCID 89676972 | 84.6% |
Reaction Steps
A 100 mL round-bottom flask was charged with 2-chloro-6-(pyrrolidin-1-yl)benzaldehyde (1.40 g, 6.68 mmol, 1.10 equiv), tert-butyl piperazine-1-carboxylate (1.13 g, 6.07 mmol, 1.00 equiv), 1,2-dichloroethane (20 mL). The mixture was stirred 30 min at room temperature. Sodium triacetoxyborohydride (3.85 g, 18.2 mmol, 2.99 equiv) was added. The resulting solution was stirred overnight at room temperature and diluted with 1,2-dichloroethane (20 mL). The resulting solution washed with H2O (2×20 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on a silica gel column with ethyl acetate/petroleum ether (3/7) to yield 1.95 g (77% yield) of tert-butyl 4-[[2-chloro-6-(pyrrolidin-1-yl)phenyl]methyl]piperazine-1-carboxylate as yellow oil. LCMS (ESI, m/z): 380 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133148B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-c2e5676f730f49dfbb250e0ccc5465c5 |
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| Source note | uspto-grants-2015_09 |
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