Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482264Generated: October 25, 2026

Fmoc-Asp(OAll)-OH → HCID 10529786, compound

https://huagongshe.com/reaction/1482264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFmoc-Asp(OAll)-OHHCID 10715692—
Reactant2-Phenylpropan-2-yl 2,2,2-trichloroacetimidateHCID 11140517—
SolventDichloromethaneHCID 6344—
ProductHCID 10529786HCID 1052978693%

Reaction Steps

2-Phenylpropan-2-yl 2,2,2-trichloroacetimidate separately synthesized by a conventional method (2.17 g, 7.74 mmol) was added to a solution of (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid (Compound 106) (1.80 g, 4.55 mmol) in dichloromethane (40 ml), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/0→65/35) to afford 4-allyl 1-(2-phenylpropan-2-yl) (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)succinate (Compound 107) (2.17 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409952B2
Source datasetuspto-grants-2016_08
ORD IDord-6e093786928743a3b2a6901df136399a
Source noteuspto-grants-2016_08