HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187817Generated: October 25, 2026
Sodium Hydroxide → 1-(4-ethylbenzyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine
https://huagongshe.com/reaction/2187817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Ethylbenzaldehyde | HCID 20861 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine | HCID 54359471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | 1-(4-ethylbenzyl)-4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine | HCID 69214536 | 62.1% |
Reaction Steps
To A solution of 4-[{N-(9-fluorenylmethyloxycarbonyl)glycyl}aminomethyl]piperidine (1.00 g, 2.33 mmol) in 2.5% AcOH/CH3OH (80 mL) were added 4-ethylbenzaldehyde (1.09 g, 8.16 mmol) and NaBH3CN (6.59 g, 10.5 mmol). The reaction mixture was stirred at 60° C. for 13 h. After the mixture was cooled to room temperature, 1 N aqueous NaOH solution (50 mL) and dichloromethane (50 mL) were added. The organic layer was separated and the aqueous layer was extracted with dichloromethane (50 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Column chromatography (SiO2, CH3OH/AcOEt 2:8) afforded 1-(4-ethylbenzyl)-4-[{N-(9-fluorenylmethyloxycarbonyl)glycyl}aminomethyl]piperidine (740 mg, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06410566B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-cc844c6e573849f6936b3540a4bea5ee |
|---|
| Source note | uspto-grants-2002_06 |
|---|