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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253191Generated: October 29, 2026

Diethyl Ether → HCID 86597314, compound

https://huagongshe.com/reaction/253191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 11243775HCID 11243775—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86597314HCID 8659731419.2%

Reaction Steps

To the product of Example 283A (69 mg, 0.224 mmol) in 3 mL 10% EtOH in EtOAc was added p-toluenesulfonic acid (p-TsOH.H2O, 45 mg, 0.24 mmol) in 2 mL 10% EtOH in EtOAc. Diethyl ether (1 mL) was added and the mixture stirred at ambient temperature until a precipitate formed. Filtration yielded 28 mg of the title compound (0.043 mmol, 19% yield). 1H NMR (CH3OH-d4, 300 MHz) δ 2.35 (s, 6H), 2.92 and 2.98 (rotamer s, 3H), 3.19 (m, 3H) 3.38 (m, 3H), 3.63 (m, 3H), 3.77 (s, 3H), 3.98 (m, 1H), 6.50 (m, 1H), 6.52 (s, 1H), 7.16 (m, 1H), 7.22 (m, 5H), 7.32 (m, 2H), 7.42 (m, 2H), 7.70 (m, 4H); MS (DCl/NH3) m/z 309 (M+H)+; Anal. calculated for C20H24N2O.2C7H8O3S: C, 62.55; H, 6.18; N, 4.29. Found: C, 62.17; H, 5.95; N, 4.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872010B2
Source datasetuspto-grants-2011_01
ORD IDord-a30ec39560ef4030a53b92a6c4c650fc
Source noteuspto-grants-2011_01