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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632747Generated: November 3, 2026

4-Toluenesulfonyl chloride → HCID 20442238, compound

https://huagongshe.com/reaction/1632747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant22212-18-6HCID 372442—
SolventPyridineHCID 1049—
ProductHCID 20442238HCID 2044223866.5%

Reaction Steps

p-Toluenesulfonyl chloride (1.2 g) was added to a stirred solution of 2,3-di-n-octyloxy-1-propanol (930 mg) in dried pyridine (10 ml) at 2° C. over 7 minutes. The reaction mixture was stirred at 0° to 5° C. for 2 hours and at room temperature overnight. The resultant solution was poured into ice water (50 ml) and extracted with ethyl acetate (40 ml). The extract was washed with dil. hydrochloric acid (20 ml) and a saturated aqueous solution of sodium chloride (20 ml) in turn, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give oil (920 mg) of 2,3-di-n-octyloxy-1-propyl p-toluenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477447
Source datasetuspto-grants-1984_10
ORD IDord-a477e2fb8d354451b9a7931e2bb67a30
Source noteuspto-grants-1984_10