HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(4-ethyl-3-methoxyphenyl)acetate → HCID 21079760, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(4-ethyl-3-methoxyphenyl)acetate | HCID 21079761 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21079760 | HCID 21079760 | 71.1% |
Reaction Steps
A solution of ethyl 4-ethyl-3-methoxyphenylacetate (4f; 3.0 g; 13.50 mmol) and CH2Cl2 (80 mL) cooled to −78° C. and a solution of (5.10 mL; 53.94 mmol; 1.0 M in CH2Cl2) over 30 min. After 1 at −78° C. the reaction was allowed to warm to rt and stirred for 12 h. The reaction was cooled in an ice-water bath and the reaction quenched with 20 mL of water. The aqueous phase was extracted with CH2Cl2:EtOAc (4:1 v/v), dried (Na2SO4), filtered and evaporated. The crude product was purified by silica gel chromatography and eluted with a CH2Cl2:EtOAc gradient (100:1→100:4) to yield 5b (2.0 g; 71%): m.s. 209.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208509B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-2b801a3f6eaa471bb2c41814179dde53 |
| Source note | uspto-grants-2007_04 |