HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223735Generated: October 30, 2026
Diethyl Ether → 4-Benzyl-1-(2-benzyloxycarbonylamino-ethyl)-piperidine-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2223735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
| Reactant | Ethyl 4-benzylpiperidine-4-carboxylate | HCID 53297794 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyl-1-(2-benzyloxycarbonylamino-ethyl)-piperidine-4-carboxylic acid ethyl ester | HCID 59715929 | — |
Reaction Steps
4-Benzyl-piperidine-4-carboxylic acid ethyl ester (2.5 g, 10 mmol), (2-bromo-ethyl)-carbamic acid benzyl ester (2.58 g, 10 mmol) and DIPEA (1.7 mL, 10 mmol) are dissolved in THF (50 mL) and heated at 80° C. for 15 h. The mixture is poured into Et2O (200 mL) and washed with sat. Na2CO3 (50 mL). The ether phase is extracted with 1M aqueous HCl (3×50 mL), the aqueous extracts washed with ether (50 mL) and adjusted to pH 14 with cooled 33% aqueous NaOH. The aqueous phase is extracted with CH2Cl2 (4×50 mL). The organic extracts are dried (Na2SO4), filtered and evaporated to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07375227B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-6321cd404e1d42c98e78b5a8598096aa |
|---|
| Source note | uspto-grants-2008_05 |
|---|