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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73456Generated: October 27, 2026

Iodoethane → Ethyl 4-(3-(2,6-dimethylbenzyloxy)phenyl)butanoate

https://huagongshe.com/reaction/73456

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 numberUS08829058B2
Source datasetuspto-grants-2014_09
ORD IDord-c68836ac96ba44e3941fcfd3f2f0f56a
Source noteuspto-grants-2014_09