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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259412Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 58380558, compound

https://huagongshe.com/reaction/1259412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(Oxetan-3-yl)ethan-1-olHCID 10844345—
SolventPyridineHCID 1049—
ProductHCID 58380558HCID 5838055856.2%

Reaction Steps

Using the same reaction conditions and procedure as described for the preparation of Intermediate (I-16a), 2-(oxetan-3-yl)ethanol (1 g, 6.944 mmol) was reacted with p-Toluene sulfonyl chloride (1.9 g, 10.416 mmol) in dry pyridine (10 mL) to afford the crude product. The reaction mass was poured into ice-water and extracted using ethyl acetate. The organic layer was washed with 1N HCl, brine solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude product. Purification by column chromatography on silica gel (20% ethyl acetate in hexane) afforded 1 g of the product (40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466289B2
Source datasetuspto-grants-2013_06
ORD IDord-25a6addfa0b04fc1b7f5f7ab3a18309c
Source noteuspto-grants-2013_06