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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673210Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → HCID 67019962, compound

https://huagongshe.com/reaction/1673210

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 67023905HCID 67023905—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 67019962HCID 67019962—

Reaction Conditions

Temperature104 °C

Reaction Steps

To the product of Step A this example (192 mg, 0.382 mmol) was added p-toluenesulfonic acid monohydrate (72.6 mg, 0.276 mmol) in toluene (3 mL). The reaction was heated to 104° C. After 80 min the reaction was cooled and diluted with EtOAc. The solution was washed with brine and saturated aq NaHCO3. The concentrated residue was purified by flash chromatography on silica gel gradient eluted with 0-25% EtOAc in hexane affording the title compound as the faster eluting isomer on silica gel. (LC-2) HPLC/MS: 502.1 (M+1), 504.1 (M+3); Rt=4.52 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999107B2
Source datasetuspto-grants-2011_08
ORD IDord-f902d558a5fd4091bb5688c471267046
Source noteuspto-grants-2011_08