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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634711Generated: November 1, 2026

Pyridine → HCID 13187521, compound

https://huagongshe.com/reaction/634711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Methylbenzenesulphonyl chlorideHCID 2734595—
Reactant2-(Cyclopentyloxy)ethan-1-olHCID 13187520—
ProductHCID 13187521HCID 1318752173%

Reaction Steps

2-Cyclopentyloxyethanol (4.3 g, 33.1 mmol) in pyridine (18 ml) was added dropwise to a solution of 3-toluenesulphonyl chloride (6.8 g, 35.7 mmol) in pyridine (27 ml) at 5° C. The mixture was allowed to warm to ambient temperature, and stirred overnight. The mixture was poured onto ice containing concentrated hydrochloric acid (46 ml) and the product was extracted with ether. The organic phase was washed with 2M hydrochloric acid, dried (MgSO4) and the solvent removed by evaporation to give 2-cyclopentyloxyethyl 4-toluenesulphonate (6.9 g, 73%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-cd77fb3878904afc8634985bf4a3df0d
Source noteuspto-grants-2001_02