Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dimethylphenol | HCID 7267 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Diphenyl sulfide | HCID 8766 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-2,5-xylenol | HCID 70756 | 97.8% |
Reaction Steps
To a solution of 100 g (0.82 mol) of 2,5-xylenol and 0.9 g of diphenyl sulfide in 700 mL of dichloromethane was added a solution of 106 g (0.79 mol) of sulfuryl chloride in 100 mL of dichloromethane, maintaining the temperature at 5-15° C. The mixture was stirred for an additional hour and then poured onto 400 g of ice-water containing 5 g of sodium bisulfite. The layers were separated, and the organic phase was washed with water, dried (MgSO4), and concentrated to dryness. The crude solids were slurried with a minimum amount of hexanes, filtered, and suction-dried to give 121 g (94%) of product, homogeneous by Thin Layer Chromatography (TLC), GC, and 1H-NMR analysis. 1H-NMR (CDCl3) δ 2.18 (s, 3H), 2.27 (s, 3H), 4.61 (s, 1H), 6.63 (s, 1H), 7.07 (s, 1H). Lit (Blackstock, Aust. J. Chem. 1973, 26, 775): mp 74-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489517B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-1aa87337794c4356abec21a45ce0ad11 |
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| Source note | uspto-grants-2002_12 |
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