Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380138Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 18367277, compound

https://huagongshe.com/reaction/380138

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-MethoxytetraloneHCID 36620—
ReactantHCID 541979HCID 541979—
SolventTolueneHCID 1140—
ProductHCID 18367277HCID 1836727746.4%

Reaction Steps

A solution of 5-methoxy-1-oxo-1,2,3,4-tetrahydronaphthalene (0.67 g), 1-(4,5-diphenyloxazol-2-yl)ethylamine (0.98 g) and p-toluenesulfonic acid (catalytic amount) in toluene (30 ml) was refluxed for 7 hours with Dean-stark equipment. The solution was evaporated in vacuo and methanol (MeOH) (10 ml) was added to the residue. To the MeOH solution, NaBH4 (0.21 g) was added at 0° C. After being stirred for 2 hours at room temperature, the solution was evaporated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was washed with brine. The dried solvent was evaporated in vacuo, and the residue was purified by chromatography on silica gel to give 1-[1-(4,5-diphenyloxazol-2-yl)ethylamino]-1,2,3,4-tetrahydro-5-methoxynaphthalene (0.73 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-5e0cd79afafd4413a189599b46a2867a
Source noteuspto-grants-2001_10