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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707632Generated: October 27, 2026

Pyridine → Oleoyl Serinate

https://huagongshe.com/reaction/707632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-[tert-butoxycarbonyl]-L-serineHCID 98766—
ReactantOleoyl chlorideHCID 5364783—
ReactantN-Oleoyl-L-SerineHCID 44190514—
SolventChloroformHCID 6212—
ProductOleoyl SerinateHCID 86669080—

Reaction Steps

0.03 moles of N-Boc-serine was constantly stirred under nitrogen in 100 mL of chloroform. 0.03 mole of oleoyl chloride was dissolved with 100 mL of chloroform and added to this heterogeneous mixture of N-Oleoylserine and followed by adding 10 mL of anhydrous pyridine. The reaction for 30 minutes under constantly stirring at room temperature, the mixture turned to homogeneous and the reaction was completed when no detectable oleoyl chloride was in the mixture. The bulk solvent was removed under vacuum and the crude product was used to next step without further purification. The resulting product (% of yields 75-80) is showed in Chemical Structure 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175027B2
Source datasetuspto-grants-2015_11
ORD IDord-87d9fddef19543e4a731086e5c1d76b5
Source noteuspto-grants-2015_11