HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099585Generated: October 25, 2026
Methyl phenylacetate → Methyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetate
https://huagongshe.com/reaction/2099585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl phenylacetate | HCID 7559 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 1-benzyl-5-ethoxy-3,4-dihydro-2H-pyrrolium tetrafluoroborate | HCID 86602992 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetate | HCID 68800975 | — |
Reaction Steps
Lithium hexamethyldisilazide solution (8.39 mL of 1M in tetrahydrofuran, 8.39 mmol) was added to dry THF and cooled to −78° C. Methyl phenylacetate (1.15 mL, 7.99 mmol) was added dropwise, and the reaction stirred for 15 minutes. A solution of 1-benzyl-5-ethoxy-3,4-dihydro-2H-pyrrolium tetrafluoroborate in 5 mL of tetrahydrofuran was added dropwise, and after one hour the reaction was allowed to warm to room temperature. The mixture was quenched with saturated NaHCO3 solution, warmed to ambient temperature and poured into water. The aqueous layer was extracted with EtOAc and the organic extract was washed with brine, dried with Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (25-30% EtOAc/hexane), providing methyl 2-(1-benzylpyrrolidin-2-ylidene)(phenyl)acetate. ESI+MS: 308.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07569589B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-df6d0ed43c554512bdff51d82061937b |
|---|
| Source note | uspto-grants-2009_08 |
|---|