HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926948Generated: October 26, 2026
Methanol → 1-(Fluoromethylsulfinyl)-4-methylbenzene
https://huagongshe.com/reaction/926948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (Fluoromethyl)(p-tolyl)sulfane | HCID 13790678 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Fluoromethylsulfinyl)-4-methylbenzene | HCID 325134 | 88% |
Reaction Steps
(Fluoromethyl)(p-tolyl)sulfane (52.09 g, 320.06 mmol) was added to a mixture of methanol (250 mL) and water (50 mL). The resulting mixture was cooled to a temperature between 0° C. and 5° C. NBS (68.36 g, 1.2 eq) was added in small portions, maintaining the same temperature range. The reaction mixture was stirred at the same temperature range until the reaction was complete. After that, the reaction mixture was quenched by the addition of Na2SO3 (10%, 150 mL). The pH of the reaction mixture was adjusted to a value between 7 and 8, with saturated NaHCO3 solution. The mixture was concentrated under vacuum at a temperature between 20° C. and 25° C. The residue was extracted with dichloromethane (200 mL, 150 mL). The combined organic layer was washed with water (2×300 ml) and concentrated to ⅓ of the volume. Heptane (50 mL) was added and then removed by distillation. The crude product was purified by flash chromatography (Ethyl Acetate/Hexane 30:70) to give 48.32 g (88%) of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290446B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-bff6af30a7a64fbd8512c077755d063e |
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| Source note | uspto-grants-2016_03 |
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