HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885373Generated: October 30, 2026
Sodium hydride → {3-[4-Chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester
https://huagongshe.com/reaction/885373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2H-1,3-oxazol-2-id-4-one | HCID 53249566 | — |
| Reactant | [3-(2-Bromomethyl-4-chloro-phenoxy)-4-methoxy-phenyl]-acetic acid ethyl ester | HCID 58237456 | — |
| Product | {3-[4-Chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester | HCID 58237617 | — |
Reaction Steps
[3-(2-Bromomethyl-4-chloro-phenoxy)-4-methoxy-phenyl]-acetic acid ethyl ester (0.15 g, 0.36 mmol), 2-oxazolidone (0.063 g, 0.72 mmol), and sodium hydride (60% in mineral oil; 0.03 g, 0.72 mmol) were combined in 1,4-dioxane (10 mL) and stirred at 80° C. for 2 hours. The mixture was cooled to room temperature to give the title compound, which was used directly as a crude solution in the hydrolysis step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242145B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-16004f9eb3a44caf93a3b1083b78ff83 |
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| Source note | uspto-grants-2012_08 |
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