Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902967Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → HCID 86599903, compound

https://huagongshe.com/reaction/902967

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 11293451HCID 11293451—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86599903HCID 8659990394%

Reaction Steps

The product of Example 18A (150 mg, 0.32 mmol) was dissolved in ethyl acetate (5 mL) and ethanol (0.2 mL), then p-toluenesulfonic acid monohydrate (122 mg, 0.64 mmol; Aldrich) was added. After stirring the mixture for 16 hours, the resulting solid was collected by filtration to afford the title compound (245 mg, 0.30 mmol; 94%). 1H NMR (300 MHz, methanol-d4): δ 7.89 (2H, d, J=8 Hz), 7.70 (4H, d, J=8 Hz), 7.47 (2H, d, J=2 Hz), 7.34 (1H, d, J=2 Hz), 7.32 (2H, dd, J=8, 2 Hz), 7.22 (4H, d, J=8 Hz), 5.04 (2H, m), 3.87 (2H, m), 3.5-3.28 (12H, m), 2.55 (2H, m), 2.40-2.21 (7H, m), 2.21-1.83 (5H, m). MS (DCl/NH3): m/z 467 (M+1)+. Anal. Calcd. for C25H30N2O3.2C7H8O3S.0.5H2O: C, 58.59; H, 5.78; N, 3.42. Found: C, 58.58; H, 5.84; N, 3.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365193B2
Source datasetuspto-grants-2008_04
ORD IDord-6596ed8c2245483d91430cad0d7c894b
Source noteuspto-grants-2008_04