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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901582Generated: November 1, 2026

1,3-Cyclohexadiene → HCID 54467431, compound

https://huagongshe.com/reaction/1901582

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexadieneHCID 11605—
ReactantHCID 75577546HCID 75577546—
ProductHCID 54467431HCID 5446743187%

Reaction Steps

N-(2-Phenylethylidene)methylamine N-oxide (797 mg, 5.34 mmol) and 1,3-cyclohexadiene (3 ml) were heated together at 70° C. in a sealed tube under nitrogen for 14 hours. The solution was cooled to room temperature and the excess 1,3-cyclohexadiene was removed under reduced pressure to yield a viscous oil (1.07 g, 87%). This crude product was purified by flash chromatography using 60:40 v/v petroleum ether (fraction of bp 40°-60° C.):ethyl acetate as the solvent system to give the title compound (Rf=0.34) as a pale yellow oil (375 mg, 35%), υmax (film) 3030, 2920, 2840, 1605, 1495, 1455, 1090 cm-1 ; δH (400 MHz; CDCl3 -Me4Si) 1.80-2.00 (4H, br m), 2.20-2.25 (1H, m), 2.60-2.65 (3H, s), 2.75-2.95 (2H and 1H, m), 4.20-4.25 (1H, br), 5.6-6.0 (2H, br m), 7.20-7.30 (5H, br m); M/z 229 (MH+ 100%) (Found: MH+ 230.1545; C15H19NO requires MH+ 230.1574).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578626
Source datasetuspto-grants-1996_11
ORD IDord-30a24b64053a42e891d553c2b6513935
Source noteuspto-grants-1996_11