HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240216Generated: October 31, 2026
Hydrochloric Acid → Ethyl (2-fluoro-4-nitrophenyl)acetate
https://huagongshe.com/reaction/2240216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Dimethyl 2-(2-fluoro-4-nitrophenyl)malonate | HCID 53429620 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (2-fluoro-4-nitrophenyl)acetate | HCID 56776686 | — |
Reaction Steps
500 mg (1.84 mmol) of dimethyl (2-fluoro-4-nitrophenyl)malonate are dissolved in 10 ml of DMSO. 33.2 mg (1.84 mmol) of water and 313 mg (7.37 mmol) of lithium chloride are added, and the mixture is heated at 100° C. for 3 hours. The reaction solution is then poured into 30 ml of ethyl acetate and shaken with saturated sodium chloride solution and with dilute hydrochloric acid. The mixture is dried over sodium sulfate and the solvent is removed under reduced pressure. The oil obtained is purified by preparative HPLC. The product fractions are extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate and the solvent is removed under reduced pressure. This gives an oil which, after seeding with product crystals, quickly crystallizes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723347B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-9e0ec4a134a94e80b6b2110756aabd4d |
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| Source note | uspto-grants-2010_05 |
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