HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388261Generated: October 28, 2026
Methyl iodide → Ethyl 2-methoxy-2-(quinolin-5-yl)acetate
https://huagongshe.com/reaction/388261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-hydroxy-2-(quinolin-5-yl)acetate | HCID 59185877 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-methoxy-2-(quinolin-5-yl)acetate | HCID 59185932 | 57% |
Reaction Steps
To a solution of ethyl 2-hydroxy-2-(quinolin-5-yl)acetate (1.5 g, 6.5 mmol) in anhydrous THF in an oven-dried flask under argon was added iodomethane (1.2 mL, 19.2 mmol) and the mixture was cooled over an ice bath. NaH (60% in oil; 0.26 g, 6.5 mmol) was added and the mixture stirred for 1 hour over ice. After removing the ice bath, stirring was continued for an additional 3.25 hours, and more NaH (60%; 0.030 g, 0.75 mmol) was added. The mixture was stirred for 45 minutes then the reaction was quenched with brine and further diluted with water. The aqueous mixture was extracted with EtOAc and the combined organics were washed with water three times, brine once, dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (50% EtOAc-hexanes) gave ethyl 2-methoxy-2-(quinolin-5-yl)acetate as a yellow oil (0.9 g, 57% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377930B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d263e518edd74002a1df0563705a682c |
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| Source note | uspto-grants-2013_02 |
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