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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723041Generated: November 1, 2026

Pyridine → HCID 88522902, compound

https://huagongshe.com/reaction/1723041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 14236874HCID 14236874—
SolventCyclohexane ethylacetateHCID 21867204—
ProductHCID 88522902HCID 8852290254%

Reaction Steps

A solution of 4.5 g (13.2 mmole) of 1,1-bis(benzoyloxymethyl)-2-hydroxymethylcyclopropane in 50 ml of dry pyridine was treated with 7 g (37 mmoles) of p-tosyl chloride and stirred at 22° for 1.5 hours. TLC in cyclohexane-ethyl acetate (2:1) (Rf 0.6) indicated that the reaction was complete. The reaction was concentrated and the residue was dissolved in 150 ml of EtOAc and washed with 50 ml of water, 100 ml saturated NaHCO3, four 250 ml portions of water and 50 ml of saturated NaCl. The ethyl acetate layer was dried (MgSO4), filtered and concentrated to 9 g of residual solid. The crude product was chromatographed on 500 ml of silica gel in cyclohexane-ethyl acetate (5:1). Fractions containing only product were combined and concentrated to give 3.36 g (54%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859680
Source datasetuspto-grants-1989_08
ORD IDord-773204a63e7f4131886100948d3e5443
Source noteuspto-grants-1989_08