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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTetrahydrofuranHCID 8028—
ReactantHexamethylphosphoramideHCID 12679—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 3-(2,6-dimethylbenzyloxy)phenylacetateHCID 66875723—
ProductEthyl 4-(3-(2,6-dimethylbenzyloxy)phenyl)butanoateHCID 66875682—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115072B2
Source datasetuspto-grants-2015_08
ORD IDord-3de7017e18fe4de7921724ee3a05bbf3
Source noteuspto-grants-2015_08