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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680527Generated: November 2, 2026

Hexane → HCID 178469478, compound

https://huagongshe.com/reaction/1680527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactantdiethyl N-(3-oxo-1-cyclohexen-1-yl)-aminomethylenemalonateHCID 12877078—
SolventDiphenyl EtherHCID 7583—
ProductHCID 178469478HCID 17846947876.1%

Reaction Steps

Diphenyl ether (20 ml) was heated to 260° C. or above, and a solution of 6.87 g of N-(3-oxo-1-cyclohexen-1-yl)aminomethylenemalonic acid diethyl ester in 5 ml of diphenyl ether was added thereto drop by drop. The resulting reaction mixture was refluxed for 15 minutes. After being allowed to cool, the reaction mixture was poured into 300 ml of n-hexane. The precipitate so formed was separated by filtration and then purified to obtain a yield of 4.37 g of the desired compound in the form of a pale-yellow powder. This compound melted (and decomposed) at 221°-224° C. Its infrared absorption spectrum (KBr tablet) had absorption peaks at 3340, 2960, 1740, 1690, 1635, 1605, 1560, 1510, 1285, 1170, 1150, 1090, 1035, 920 and 815 cm-1, and its n.m.r. spectrum (d6 -DMSO, 60Mc, TMS) had signals at δ values of 1.31 (3H, t, J=7 Hz), 1.9-3.1 (6H, m), 4.27 (2H, q, J=7 Hz), and 8.55 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273932
Source datasetuspto-grants-1981_06
ORD IDord-15388353c75f4f5fb470d1f4c6d561f7
Source noteuspto-grants-1981_06