HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278185Generated: November 1, 2026
tert-Butyl piperazine-1-carboxylate → HCID 89676941, compound
https://huagongshe.com/reaction/2278185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Fluoro-2-(morpholin-4-yl)benzaldehyde | HCID 26188751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89676941 | HCID 89676941 | 121.4% |
Reaction Steps
A 50 mL round-bottom flask was charged with 3-fluoro-2-(morpholin-4-yl)benzaldehyde (0.500 g, 2.39 mmol, 1.00 equiv), tert-butyl piperazine-1-carboxylate (404 mg, 2.17 mmol, 0.91 equiv), dichloromethane (10 mL). The mixture was stirred at room temperature for 0.5 hour. Sodium triacetoxyborohydride (1.38 g, 6.51 mmol, 2.72 equiv) was added. The resulting solution was stirred overnight at room temperature and diluted with dichloromethane. The resulting mixture was washed with H2O (3×10 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 (1/3) to yield 1.00 g (crude) of tert-butyl 4-[[3-fluoro-2-(morpholin-4-yl)phenyl]methyl]piperazine-1-carboxylate as colorless 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-f5091fd4ee3642d581b38322fd6627fa |
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| Source note | uspto-grants-2015_09 |
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