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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747930Generated: October 31, 2026

Diethyl Ether → HCID 86597314, compound

https://huagongshe.com/reaction/747930

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 numberUS07399765B2
Source datasetuspto-grants-2008_07
ORD IDord-83220a29184b43df8abb789b35881440
Source noteuspto-grants-2008_07