HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459795Generated: October 26, 2026
Potassium Acetate → 2-Bromo-6-nitrobenzyl Acetate
https://huagongshe.com/reaction/459795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 1-Bromo-2-(bromomethyl)-3-nitrobenzene | HCID 15063170 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-6-nitrobenzyl Acetate | HCID 58824122 | — |
Reaction Steps
To a solution of 1-bromo-2-bromomethyl-3-nitro-benzene (3.39 g, 11.53 mmol) in DMF (50 nml) was added KOAc (7.6 g, 77.4 mmol). The reaction was heated at 70° C. for an hour. After cooling to room temperature, the mixture was partitioned between water and ethyl acetate. The organic layer was washed with water and brine, and dried over MgSO4 Acetic acid 2-bromo-6-nitro-benzyl ester (3.1 g) was obtained as a brown oil after concentration under vacuum (˜100%). 1H NMR (CDCl3, 300 MHz) δ: 2.06(s, 3H), 5.46 (s, 2H), 7.377(t, J=8.1 Hz), 7.778(dd, J=1.23 Hz, 8.14 Hz), 7.856(dd, J=1.23 Hz, 8.07 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196087B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-2b245187379b4f5c91e535abb54e0584 |
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| Source note | uspto-grants-2007_03 |
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