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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597850Generated: October 30, 2026

Triethylamine → HCID 54205135, compound

https://huagongshe.com/reaction/597850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzenepropanoyl chlorideHCID 64801—
ReactantHCID 54205135HCID 54205135—
SolventAcetoneHCID 180—
ProductHCID 54205135HCID 54205135—
ProductHCID 86634869HCID 86634869—

Reaction Steps

Farnesyl-L-Cysteine methyl ester (FCM) was synthesized as described in Ma et al., Methods Enzymol. 250, 226-34 (1995). The FCM (1 g) was dissolved in approximately 100 ml of acetone followed by the addition of triethylamine (TEA, 1 ml) and 1 g of hydrocinnamoyl chloride. This was stirred for 2 h at room temperature. The solvent was removed under reduced pressure, the residue dissolved in 150 ml of ethylacetate and washed three times with water. The ethylacetate layer was dried with anhydrous sodium sulfate, filtered and the ethylacetate removed under reduced pressure. The residue was purified by silica gel chromatography to obtain hydrocinnamoyl-farnesyl-L-Cysteine methyl ester (HCFCM). The purified HCFCM was then analyzed by Electron Spray Ionization Mass Spectrometry (ESI-MS).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897604B2
Source datasetuspto-grants-2011_03
ORD IDord-e55cd67340af44ccab044c7506a21cfa
Source noteuspto-grants-2011_03