HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098965Generated: October 31, 2026
Methyl (trimethylsilyl)acetate → (E)-Methyl 2-(6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-ylidene)acetate
https://huagongshe.com/reaction/2098965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl (trimethylsilyl)acetate | HCID 76210 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 6-(Benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-one | HCID 59590882 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (E)-Methyl 2-(6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-ylidene)acetate | HCID 59590938 | 45% |
Reaction Steps
At −78° C., lithium bis(trimethylsilyl)amide (1.0 M in THF) (3.6 mL, 3.6 mmol) was added slowly to a solution of methyl 2-(trimethylsilyl)acetate (0.59 mL, 3.6 mmol) in THF (20 mL). The mixture was maintained at −78° C. for 7 minutes and then 6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-one (8.3) (0.535 g, 2.0 mmol) was added in one portion. The resulting mixture was stirred at −78° C. and allowed to warm to room temperature overnight. The reaction mixture was then diluted with EtOAc (200 mL), washed with water and brine, and dried over anhydrous sodium sulfate. After removing solvent, the residue was purified by chromatography (silica gel, 1:5 EtOAc/hexane) to give product 8.4 in 45% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08450522B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-49a907eaa4cc4f1ea9d5b4248f92bb8d |
|---|
| Source note | uspto-grants-2013_05 |
|---|