Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779187Generated: November 1, 2026

Malonic Acid → (E)-10-heptyloxy-dec-3-enoic acid

https://huagongshe.com/reaction/1779187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalonic AcidHCID 867—
ReactantTriethylamineHCID 8471—
ReactantMonosodium phosphateHCID 23672064—
Reactant8-Heptyloxy-octanalHCID 90060147—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(E)-10-heptyloxy-dec-3-enoic acidHCID 90060136100.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

Under a nitrogen atmosphere, 8-heptyloxy-octanal (178.0 mg, 0.734 mmol) obtained in Step D-2 was dissolved in toluene (3.56 mL), and triethylamine (184 μL, 1.32 mmol) and a solution of malonic acid (137.6 mg, 1.32 mmol) in DMF (0.178 mL) were added in order at 75° C. The mixture was stirred at 90° C. for 16 hours. After cooling to room temperature, an aqueous solution (2.6 mL) of 30% sodium dihydrogen phosphate and ethyl acetate (5.2 mL) were added, and the mixture was stirred at room temperature for 5 minutes. After extraction, the organic layer was washed with water. The aqueous layer was washed with ethyl acetate. The combined organic layer was then washed again with water and a saturated brine, dried over anhydrous sodium sulfate, and then filtered. The solvent was distilled off to obtain 209.7 mg (quant.) of (E)-10-heptyloxy-dec-3-enoic acid (ESI (LC/MS positive mode) m/z 285 (M+H); Rt 2.23 min.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266853B2
Source datasetuspto-grants-2016_02
ORD IDord-156c8fdae8a240ebaac208d542079bab
Source noteuspto-grants-2016_02