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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489065Generated: October 30, 2026

Pyridine → Benzyl-5-(N-FMOC-L-valyloxy)-4-stearoyloxy-2-pentenoate

https://huagongshe.com/reaction/489065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantStearoyl chlorideHCID 8212—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl 5-(N-FMOC-L-valyloxy)-4-hydroxy-2-pentenoateHCID 54039988—
SolventDichloromethaneHCID 6344—
ProductBenzyl-5-(N-FMOC-L-valyloxy)-4-stearoyloxy-2-pentenoateHCID 53974693—

Reaction Steps

To a solution of benzyl-5-(N-FMOC-L-valyloxy)-4-hydroxy-2-pentenoate (6.5 g, 12 mmol) and pyridine (2.0 g, 25 mmole) in 100 ml dichloromethane at 10° C. was added dropwise a solution of stearoylchloride (4.55 g, 15 mmol) in 25 ml dichloromethane. The mixture was stirred overnight. 100 ml of 5% sodium hydrogencarbonate solution was added and the mixture was stirred for 30 minutes. The organic phase was seperated and the water phase was extracted two times with dichloromethane. The combined organic phases were dried with sodium sulfate and concentrated in vacuo. The product was isolated by silica gel column chromatography Yield: 7.8 g=80%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974802B2
Source datasetuspto-grants-2005_12
ORD IDord-19e81bfb599546b39faf657550c72823
Source noteuspto-grants-2005_12