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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322707Generated: October 29, 2026

Tert-butoxycarbonylalanine → N-[N-(Dec-4enoyl)-L-alaninyl]-L-phenylalanine Methyl Ester

https://huagongshe.com/reaction/322707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantL-Phenylalanine, methyl esterHCID 736234—
ReactantAlanylphenylalanine methyl esterHCID 12988705—
ProductN-[N-(Dec-4enoyl)-L-alaninyl]-L-phenylalanine Methyl EsterHCID 54300131—

Reaction Steps

Following General Procedure A and using N-(L-alaninyl)-L-phenylalanine methyl ester (prepared by coupling N-BOC-L-alanine (Sigma) and L-phenylalanine methyl ester (Sigma) using General Procedure A, followed by removal of the BOC-group using General Procedure Y) and dec-4-enoic acid prepare from ethyl dec-4enoate (ICM) using General Procedure N), the title compound was prepared as a solid (mp =115.5-117.5° C.). The reaction was monitored by tlc (Rf=0.52 in 50% EtOAc/hexanes; 0.60 in 10% CH3OH/CH2Cl2) and the product was purified by flash chromatography using 10% CH3OH/CH2Cl2 as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211235B1
Source datasetuspto-grants-2001_04
ORD IDord-1c6752b8c8aa4a28ace8a27e03593a5b
Source noteuspto-grants-2001_04