HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926961Generated: October 27, 2026
Methanol → 1-[(Chloromethyl)sulfinyl]-4-methylbenzene
https://huagongshe.com/reaction/926961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Chloromethyl p-Tolyl Sulfide | HCID 1502059 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[(Chloromethyl)sulfinyl]-4-methylbenzene | HCID 11127044 | 89.51% |
Reaction Steps
(Choromethyl)(p-tolyl)sulfane (10 g, 57.91 mmol) was added to a mixture of methanol (50 mL) and water (10 mL). The resulting mixture was cooled to a temperature between 0° C. and 5° C. NBS (12.37 g, 1.2 eq) was added in small portions, maintaining the same temperature range. The reaction mixture was stirred within the same temperature range until the reaction was complete. Thereafter, the reaction mixture was quenched by the addition of Na2SO3 (10%, 30 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. and then extracted with dichloromethane (40 mL, 30 mL). The combined organic layer was washed with water (2×60 ml) and concentrated to ⅓ of the volume. Heptane (10 mL) was added and then removed by distillation. The crude product was purified by flash chromatography (Ethyl Acetate/Hexane 30:70) to give 9.78 g (89.51%) 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-a2e90d33346b4b47a7e5075dd0edf592 |
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| Source note | uspto-grants-2016_03 |
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