HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21978Generated: October 26, 2026
tert-Butyl Dimethylphosphonoacetate → Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate
https://huagongshe.com/reaction/21978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| Reactant | Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate | HCID 19930804 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate | HCID 54383214 | — |
Reaction Steps
Potassium hexamethyldisilylamide (40.5 mL of a 0.58M solution in toluene, 23.5 mmol) is added to THF (60 mL), and then cooled to 0° C. t-Butyl dimethylphosphonoacetate (4.6 mL, 23.5 mmol) is added dropwise, and the reaction is warned to room temperature and stirred for 25 minutes. Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (2.83 g, 11.74 mmol) is added in THF (15 mL), and the reaction is stirred at room temperature for 2.5 hours. The reaction is quenched with saturated ammonium chloride, and then extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05426103 |
|---|
| Source dataset | uspto-grants-1995_06 |
|---|
| ORD ID | ord-abd37e9569de41e18c1a8ba201ccfeea |
|---|
| Source note | uspto-grants-1995_06 |
|---|