Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629621Generated: October 30, 2026

Diethylamine → 5-Methyl-2-oxo-cyclohexanecarboxylic acid diethylamide

https://huagongshe.com/reaction/1629621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantEthyl 5-methyl-2-oxocyclohexane-1-carboxylateHCID 458119—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
Product5-Methyl-2-oxo-cyclohexanecarboxylic acid diethylamideHCID 6667982865.1%

Reaction Steps

5-Methyl-2-oxo-cyclohexanecarboxylic acid ethyl ester (45) (5.9 g, 32 mmol), DMAP (1.12 g, 10 mmol) and diethylamine (4.7 g, 65 mmol, 6.7 mL) in toluene (90 mL) were heated at reflux for 4 days. The reaction was allowed to cool and the toluene was removed under reduced pressure to give a yellow oil. The crude material was purified by silica gel chromatography eluting with petrol (A) and ethyl acetate (B) (20-50% B, 80 g) to afford 4.4 g (65%) of 5-methyl-2-oxo-cyclohexanecarboxylic acid diethylamide (46) as a yellow oil. The structure was confirmed 1H NMR (300 MHz, CDCl3) δH 0.8-1.05 (9H, m, CH3 and N(CH2CH3)2), 1.05-2.10 (5H, m, 5-CH and 4- and 6-CH2), 2.15-2.80 (2H, m, 3-CH2), 2.95-3.55 (5H, m, 1-CH and N(CH2CH3)2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08790619B2
Source datasetuspto-grants-2014_07
ORD IDord-32f01ccdcb7f428bb49f7ab5a1c6522d
Source noteuspto-grants-2014_07