Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427705Generated: October 31, 2026

Sodium Hydroxide → HCID 68016188, compound

https://huagongshe.com/reaction/1427705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPropanedioic acid, 2-[2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butylidene]-, 1,3-dimethyl esterHCID 24938928—
SolventMethanolHCID 887—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductHCID 68016188HCID 68016188—

Reaction Steps

Conjugated malonate 3a (0.5 g, 1.5 mmol, from a 5% stock solution in methanol) was incubated with 375 Units Pig Liver Esterase (Sigma-Aldrich) in 100 mM potassium phosphate buffer pH 7.5, at 25 and with constant stirring. After 20 h of incubation the pH of the reaction mixture was set to 9 with 30% NaOH followed by incubation at room temperature for 30 min with constant stirring. The reaction mixture was then extracted 3 times with 250 ml tert-butyl methyl ether. The organic phase was washed twice with 125 ml deionized water and once with saturated NaCl solution, dried over Na2SO4 and finally evaporated under reduced pressure at 45° C. 0.4 g of conjugated malonate 3a were recovered. The pH of the aqueous phase left from the basic (pH 9) extraction was set to 3 with conc. HCl, Extraction with tert-butyl methyl ether, washing with water and saturated NaCl, drying over Na2SO4, filtration and evaporation under reduced pressure at 45° C. gave 62 mg (13%) of deconjugated half malonate 1a as colorless oil and E/Z 72:28 according to NMR. The suppression of byproduct 1b depends on the quality of the PLE employed, with aged PLE (>1 year) giving exclusively isomer 1a. Analytical data of the E-isomer: 1H-NMR (400 MHz, CDCl3): δ0.96 (s, 6 H), 1.56 (3 H), 1.67 (s, 3 H), 1.4 (2 H), 1.5 (2 H), 1.9 (2 H), 2.0 (4 H), 3.6 (s, 3 H, OMe), 4.2 (d, 1 H), 5.4 (d, 1 H) ppm. 13C-NMR (400 MHz, CDCl3): 16.4 (q), 19.1 (t), 19.6 (q), 27.2 (t), 28.4 (2 q), 32.3 (t), 34.6 (s), 39.3 (t), 39.7 (t), 50.9 (d), 52.2 (q), 116.3 (d), 126.8 (s), 136.3 (s), 141.0 (s), 169.1 (s), 169.6 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933253B2
Source datasetuspto-grants-2015_01
ORD IDord-0a009147e7f74933b931bb6678e09cc4
Source noteuspto-grants-2015_01