HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630963Generated: November 1, 2026
Water → Methyl 4-Bromo-3-(bromomethyl)benzoate
https://huagongshe.com/reaction/1630963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 4-bromo-3-methylbenzoate | HCID 3294148 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 4-Bromo-3-(bromomethyl)benzoate | HCID 11460987 | — |
Reaction Steps
NBS (46.6 g, 262 mmol) and AIBN (0.72 g, 4.4 mmol) were added in one portion into a solution of methyl 4-bromo-3-methylbenzoate (50.0 g, 218 mmol) in CHCl3 (1 L) under N2. The mixture was stirred at 70° C. for 2 days. The reaction mixture was cooled to RT and water (500 mL) was added. The organic layer was washed with a saturated solution of NaHCO3 (50 mL), water (350 mL) and brine (500 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure. The residue was washed with pentane (2×500 mL) affording the title compound as a yellow solid. HPLC (Method A), Rt 4.9 min (Purity: 98.2%). 1H NMR (DMSO-d6, 300 MHz) δ 8.24 (d, J=1.9 Hz, 1H), 7.85 (m, 2H), 4.87 (s, 2H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791142B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-56b7e8e180c34f548706a68478035128 |
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| Source note | uspto-grants-2014_07 |
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