HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422033Generated: October 26, 2026
Acetic Acid → Ethyl 2-(4-bromo-2-nitrophenyl)acetate
https://huagongshe.com/reaction/422033
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,3-Dimethyl 2-(4-bromo-2-nitrophenyl)propanedioate | HCID 15740596 | — |
| Product | Ethyl 2-(4-bromo-2-nitrophenyl)acetate | HCID 23247724 | — |
Reaction Steps
To a suspension of 2-(4-bromo-2-nitro-phenyl)-malonic acid dimethyl ester (crude, 8.1 mmol) in acetic acid (10 mL) is added 6N HCl (10 mL). The mixture is heated at 110° C. overnight (about 15 hr). The reaction mixture is evaporated to dryness. The crude is used in the next step without further purification. To a solution of the crude in ethanol (40 mL) is added concentrated H2SO4 (3 drops) and the resulting reaction mixture is heated at reflux over night. Solvent is removed under reduced pressure. It is purified by flash column chromatography. 1H NMR (400 MHz, CDCl3) δ 8.25 (s, 1 H), 7.72-7.7 (m, 1 H), 7.26-7.22 (m, 1 H), 4.23-4.13 (q, 2 H), 3.97 (s, 2 H), 1.29-1.23 (t, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101608B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-aa490170718c48e58721ae2e7a7b0cfe |
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| Source note | uspto-grants-2012_01 |
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