Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199392Generated: October 27, 2026

Methanol → 1-[(Chloromethyl)sulfinyl]-4-methylbenzene

https://huagongshe.com/reaction/2199392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-bromobutanimideHCID 67184—
ReactantChloromethyl p-Tolyl SulfideHCID 1502059—
SolventWaterHCID 962—
Product1-[(Chloromethyl)sulfinyl]-4-methylbenzeneHCID 1112704489.51%

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 1/3 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359294B2
Source datasetuspto-grants-2016_06
ORD IDord-8a853981ef43482a96230bd9d6ee3768
Source noteuspto-grants-2016_06