HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516832Generated: October 27, 2026
Iodoethane → Ethyl 4-(3-(2,6-dimethylbenzyloxy)phenyl)butanoate
https://huagongshe.com/reaction/516832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Ethyl 3-(2,6-dimethylbenzyloxy)phenylacetate | HCID 66875723 | — |
| Product | Ethyl 4-(3-(2,6-dimethylbenzyloxy)phenyl)butanoate | HCID 66875682 | — |
Reaction Steps
To a stirred solution of Ethyl 2-(3-(2,6-dimethylbenzyloxy)phenyl)acetate (Step A, 4.79 g, 16.0 mmol) in dry THF (60 ml) was added drop wise a solution of lithium diisopropylamide (1.0 M in THF, 25 ml) at −78° C. under argon followed by addition of hexamethylphosphoramide (HMPA, 15 ml). After 15 minutes of stirring at −78° C., Iodoethane (12.53 g, 80.3 mmol) was added rapidly. The reaction mixture was warmed to room temperature for 16 hours. The crude mixture was quenched with sat. NH4Cl and extracted with ether (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (ethyl acetate:hexane, 1:4) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115072B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-3de7017e18fe4de7921724ee3a05bbf3 |
|---|
| Source note | uspto-grants-2015_08 |
|---|