HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308899Generated: October 26, 2026
Ethyl Acetate → 2-[(2-Chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone
https://huagongshe.com/reaction/2308899
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Bromomethyl)-1-chloro-3-nitrobenzene | HCID 91858 | — |
| Reactant | 4,4-Dimethyl-1,2-oxazolidin-3-one | HCID 642151 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[(2-Chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone | HCID 13934944 | 52.7% |
Reaction Steps
A mixture of 2-chloro-6-nitrobenzyl bromide (17.5 g, 0.07 mole), 4,4-dimethyl-3-isoxazolidinone (11.5 g, 0.1 mole), potassium carbonate (13.8 g, 0.1 mole), and 1,4,7,10,13,16-hexaoxacyclooctadecane (0.5 g, 0.002 mole) in acetonitrile (500 ml) was stirred at ambient temperature overnight. The reaction mixture was poured into ethyl acetate (500 ml) and the mixture washed with water (3×200 ml). The dried (magnesium sulfate) ethyl acetate layer was concentrated under reduced pressure to yield a liquid. The liquid product was subjected to chromatography on silica gel, eluting with 1:9 ethyl acetate:heptane. The appropriate fractions were combined and concentrated under reduced pressure to yield a white solid. The solid was recrystallized from ethyl acetate to yield 10.5 g of 2-[(2-chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone, m.p. 86°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04692182 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-72a1f803fa9f4c17acf7237769c045bd |
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| Source note | uspto-grants-1987_09 |
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