HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434564Generated: October 26, 2026
Acetic Acid → 4-[4-(3-Piperidin-1-yl-propoxy)benzyl]-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1434564
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 4-(3-Piperidin-1-ylpropoxy)benzaldehyde | HCID 2766324 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 4-[4-(3-Piperidin-1-yl-propoxy)benzyl]-piperazine-1-carboxylic acid tert-butyl ester | HCID 68697319 | 50% |
Reaction Steps
To a solution of 4-(3-(piperidin-1-yl)propoxy)benzaldehyde (WO 02/12214 A2) (1.90 g, 7.68 mmol) in dichloromethane (25 ml) was added 1-N tert butoxy carbonyl piperazine (1.57 g, 8.45 mmol) followed by acetic acid (1 ml), and the reaction stirred for 1 hour at room temperature, then treated with sodium triacetoxy borohydride (2 g, 9.61 mmol) and stirred for 16 hours at room temperature. The reaction was then diluted with saturated sodium bicarbonate solution and extracted with dichloromethane. The dichloromethane was then washed sequentially with water and brine, dried over anhydrous sodium sulfate and evaporated in vacuo to yield a residue which was purified using silica gel chromatography eluting with a mixture of 0.880 ammonia:methanol:dichloromethane (0.5:4.5:95) to afford the title compound (1.586 g, 50%); MS (ES+), m/e 418 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615550B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-6bc965e3c5c84fe6903172ba8a23a8c4 |
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| Source note | uspto-grants-2009_11 |
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