Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420874Generated: October 30, 2026

Triethylamine → HCID 54205135, compound

https://huagongshe.com/reaction/420874

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 numberUS08097722B2
Source datasetuspto-grants-2012_01
ORD IDord-f8e1cc831e04459699e3d57ae0aa89fe
Source noteuspto-grants-2012_01