HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387089Generated: October 31, 2026
Methyl iodide → 4-Bromo-2-chloro-1-methanesulfonylbenzene
https://huagongshe.com/reaction/2387089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Bromo-2-chlorobenzenesulfonyl chloride | HCID 2734766 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-2-chloro-1-methanesulfonylbenzene | HCID 23093061 | 32.4% |
Reaction Steps
Hydrazine monohydrate (1.51 mL, 48 mmol) was added to a cooled 0° C. solution of 4-bromo-2-chlorobenzenesulfonyl chloride (5 g, 17.2 mmol) dissolved in THF (50 mL). The reaction was stirred at room temperature for 2 hours and then the solvent was removed in vacuo to give a white solid. The solid was dissolved in EtOH (100 mL) and treated with sodium acetate (6.56 g, 80 mmol) followed by methyl iodide (4.9 mL, 79 mmol). The reaction mixture was refluxed for 18 hours. The solvent was removed in vacuo to give a residue that was partitioned between 1 N HCl and EtOAc. The organic layer was dried over MgSO4 and concentrated. The crude mixture was purified by flash column chromatography to give the product (1.5 g, 32%). 1H NMR (300 MHz, CDCl3): δ 3.26 (s, 3H), 7.63 (dd, J=8.5, 1.9 Hz, 2 H), 7.74 (d, J=1.9 Hz, 1 H), 8.02 (d, J=8.5 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268835B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-0af07a8fc81443fd825c005c0085a5e8 |
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| Source note | uspto-grants-2012_09 |
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