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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433321Generated: November 3, 2026

Triethylamine → HCID 57935243, compound

https://huagongshe.com/reaction/1433321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant(R)-(-)-4-Methylhexanoic acidHCID 12600623—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57935243HCID 5793524347.4%

Reaction Steps

Dicyclohexyl carbodiimide (9.51 g, 46.1 mmol), N,N′-dimethyl-4-aminopyridine (1.13 g, 9.2 mmol) and triethylamine (6.4 ml, 46.1 mmol) were added to a solution of Meldrum's acid (6.64 g, 46.1 mmol) in dichloromethane (150 ml). (4R)-4-Methylhexanoic acid (6 g, 46.1 mmol) was added and the reaction mixture was stirred overnight. The reaction mixture was filtered and the solid was washed with dichloromethane (2×100 ml). The filtrate and washings were combined and evaporated under reduced pressure to give an orange oil. Acetic acid (50 ml) and water (50 ml) were added and the reaction was heated under reflux overnight. After the solution had cooled to room temperature it was extracted with pentane (100 ml). The organic extract was dried (MgSO4) and evaporated to give a residue that was purified by column chromatography on silica gel using an elution gradient of pentane to pentane:diethyl ether 19:1 to give the title compound (2.8 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612226B2
Source datasetuspto-grants-2009_11
ORD IDord-9a327db5d1dc4be4bee4597523a5ffbf
Source noteuspto-grants-2009_11