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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354895Generated: November 1, 2026

Iodoethane → 3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl ester

https://huagongshe.com/reaction/1354895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantPropionate ionHCID 104745—
Reactant3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl esterHCID 15186153—
SolventDimethylformamideHCID 6228—
Product3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl esterHCID 1107796898%

Reaction Steps

To a slurry of sodium hydride (60% suspension in oil, 7.5 g) and dimethyl formamide (70 ml) was added a solution of the racemic ethyl 2-hydroxy-3-(4-benzyloxyphenyl(propionate of the formula (10) (40 g) obtained according to the procedure described in step (iii) above in dimethylformamide (105 ml) at 5–10° C. over a period of 15–30 minutes. The temperature was allowed to attain room temperature and maintained at the same temperature for 1–3 h. Ethyl iodide (36 g) was added slowly by maintaining the temperature at 25–30° C. over a period of 2–3 h. The progress of the reaction was monitored by TLC. After completion of the reaction, the reaction mixture was dumped into ice water and extracted with toluene. The combined organic extracts were washed with water and the solvent was removed under reduced pressure to afford the title compound of the formula (12a) (47–48 g, 98–99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223881B2
Source datasetuspto-grants-2007_05
ORD IDord-4e65c20889ab4c7da4cb1a2419f3c213
Source noteuspto-grants-2007_05