HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861549Generated: October 30, 2026
Iodoethane → 3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl ester
https://huagongshe.com/reaction/1861549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester | HCID 15186153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl ester | HCID 11077968 | 98% |
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 ethyl2-hydroxy-3-(4-benzyloxy phenyl)propionate of the formula (10) (40 g) obtained according to the procedure described in step (iv) 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 25-30° C. over a period of 2-3 hours. 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 racemic 2-ethoxy ethyl ester of the formula (12a) (47-48 g, 98-99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531596B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-5595f5d3a90d483f83b46d35138e9b71 |
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| Source note | uspto-grants-2003_03 |
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