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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397624Generated: October 26, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/2397624

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-HydroxycaprylonitrileHCID 13413803—
Reactant1-amino-3(S)-octanolHCID 22797505—
Productp-Toluenesulfonic acidHCID 6101—
Product1-Amino-3(S)-(tetrahydro-2H-pyran-2-yloxy)octaneHCID 54030328—

Reaction Steps

This compound is prepared essentially by the same method as described in Example 1, Step A-2, except that the 3-hydroxycaprylonitrile is replaced by 1-amino-3(S)-octanol and slightly more than one equivalent of p-toluenesulfonic acid. hydrate is used. This method provides the p-toluenesulfonic acid salt of the title compound which is converted to the oily title compound by distribution between dilute sodium hydroxide and ether. The organic phase is washed with saturated aqueous brine, dried over sodium sulfate, and filtered. Evaporation of the filtrate in vacuo leaves the title compound as a residual oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022794
Source datasetuspto-grants-1977_05
ORD IDord-15fdaa5ece704e8285f39984a93db8c1
Source noteuspto-grants-1977_05