HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181673Generated: October 31, 2026
Allyl bromide → Methyl 4-(allyloxy)-3-iodobenzoate
https://huagongshe.com/reaction/2181673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-hydroxy-3-iodobenzoate | HCID 11346465 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(allyloxy)-3-iodobenzoate | HCID 11186196 | 60% |
Reaction Steps
Methyl 4-hydroxy-3-iodobenzoate (1.85 g, 6.65 mmol) is dissolved in anhydrous DMF (15 mL) in a dry flask under nitrogen, treated with NaH (60% dispersion in oil, 265 mg, 6.65 mmol) and stirred for 1 h at RT. Allyl bromide (633 μL, 7.32 mmol) is added and the mixture is stirred for 16 h. The mixture is concentrated and the residue is partitioned between EtOAc (25 mL) and H2O (25 mL). The organic layer is washed with a 50% saturated mixture of 1:1 NaC/NaHCO3 (2×10 mL), dried (MgSO4) and concentrated to a yellow oil which solidified to a white solid upon standing (2.12 g). The crude material is chromatographed over 100 g slurry-packed silica gel, eluting with 10% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 1.27 g (60%) of methyl 4-(allyloxy)-3-iodobenzoate as a colorless oil which solidified on standing. MS for C11H11IO3 (EI) m/z: 318 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06894042B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-5874123d145b41b18ad163ef88ad1818 |
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| Source note | uspto-grants-2005_05 |
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