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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262900Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 13877995, compound

https://huagongshe.com/reaction/1262900

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantCycloheptanolHCID 10399—
SolventPyridineHCID 1049—
ProductHCID 13877995HCID 13877995—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a one liter, four-necked, round bottom flask equipped with stirrer, condenser, and thermometer, 200.0 parts of pyridine and 28.5 parts of cycloheptanol were mixed under a nitrogen blanket and chilled to 0° C. with an ice water bath. To this solution 53.5 parts of p-toluenesulfonyl chloride were added in portions over thirty minutes. The solution was stirred for one hour at 0° C. and then allowed stand for twenty-four hours at 15° C. The mixture was poured into one liter of ice water and subsequently extracted with 700 parts of methylene chloride. The organic layer was washed successively with cold 6 N sulfuric acid (until the water layer was acidic to pH paper), dilute sodium bicarbonate (three times with 500 part-portions), and water (twice with 500 part-portions). It was then dried over sodium sulfate, filtered, and the solvent removed in vacuo to yield cycloheptyl para-toluenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454274
Source datasetuspto-grants-1984_06
ORD IDord-056d9cd1d9f548c5856dedbf29f1e3d6
Source noteuspto-grants-1984_06