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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41075Erstellt: 26. Oktober 2026

1,2-Dichloroethane → (S)-4-tert-butyl 1-((R)-2-pent-4-enamido-2-phenylethyl) 2-allylsuccinate

https://huagongshe.com/reaction/41075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktDiisopropylethylamineHCID 81531—
Edukt(S)-2-[2-(tert-Butoxy)-2-oxoethyl]pent-4-enoic AcidHCID 16053367—
Edukt(R)-N-(2-hydroxy-1-phenylethyl)pent-4-enamideHCID 67310926—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
Produkt(S)-4-tert-butyl 1-((R)-2-pent-4-enamido-2-phenylethyl) 2-allylsuccinateHCID 67310391—

Reaktionsschritte

To a solution of (S)-2-(2-tert-butoxy-2-oxoethyl)pent-4-enoic acid (684 mg, 3.19 mmol) in DMF (25 mL) cooled in an ice/water bath was added EDC (612 mg, 3.19 mmol) and the resulting solution was stirred for 30 min. (R)-N-(2-hydroxy-1-phenylethyl)pent-4-enamide (700 mg, 3.19 mmol), iPr2NEt (1.77 mL, 9.58 mmol), and DMAP (39.0 mg, 0.319 mmol) were subsequently added and the reaction mixture was stirred 16 h at which point LC-MS analysis indicated the presence of both starting material and desired product. The reaction mixture was diluted with saturated NH4Cl and EtOAc and the layers separated. The aqueous layer was extracted 2× with EtOAc and the combined organic extracts were washed with 1 N HCl and brine, dried over Na2SO4, filtered, and concentrated. The crude product was purified using silica gel chromatography (MeOH/CH2Cl2 gradient) to yield 340 mg of product as a colorless oil in 26% yield. LRMS (M+Na)+: 438.4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530456B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d71ae031ebc240d5ad4a4f7bf7f8a38e
Quellennotizuspto-grants-2013_09