HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193330Generated: October 31, 2026
Water → tert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate
https://huagongshe.com/reaction/1193330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Product | tert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate | HCID 10333298 | 78% |
Reaction Steps
A solution of tert-butyl 4-oxopiperidine-1-carboxylate (10.0 g, 50.25 mmol, 1 eq) in THF (50 ml) was added at 0° C. to a suspension of NaH (1.56 g, 65.32 mmol, 1.3 eq) in THF (50 ml), and stirring was carried out for 30 min. Triethyl phosphoroacetate (12.96 ml, 65.32 mmol, 1.3 eq) in THF (50 ml) was added dropwise, and stirring was carried out for 2 h at RT. The reaction mixture was hydrolyzed with water (5 ml) and concentrated. The residue was taken up in water (150 ml) and extracted with ethyl acetate (2×300 ml). The combined organic phases were washed with sat. NaCl solution (200 ml), dried over sodium sulfate and concentrated under reduced pressure. The crude substance was purified by column chromatography (silica gel, 3% ethyl acetate in hexane) (white solid). Yield: 78% (10.5 g, 39.03 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08680159B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-890b4d00714445caaa8887c66973b64e |
|---|
| Source note | uspto-grants-2014_03 |
|---|