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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1671394Erstellt: 26. Oktober 2026

Hydrochloric Acid → (S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidine

https://huagongshe.com/reaction/1671394

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktPhenolHCID 996—
EduktTriphenylphosphineHCID 11776—
Edukt2,3,6-TrichlorophenolHCID 13618—
EduktDiisopropyl azodicarboxylateHCID 5363146—
Edukt(S)-3-(1-Hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 58104606—
LösungsmittelTolueneHCID 1140—
Produkt(S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidineHCID 58104602—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of (S)-3-(1-hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic acid t-butyl ester (21.0 mg, 93.2 μmmol) and DIAD (22.0 μL, 112 μmmol) was dissolved in toluene (65 μL, 610 μmmol) at room temperature. PPh3 (29.3 mg, 112 μmmol) and 2,3,6-trichlorophenol (20.2 mg, 102 μmmol) were dissolved in toluene (0.1 mL, 1 mmol) and heated at 100° C. The t-butyl ester mixture was slowly added into the phenol mixture at 100° C., and stirred for 1 hour. The mixture was then removed from the heat and stirred at room temperature overnight. The mixture was then concentrated and the resulting residue was treated with 1.25M HCl in EtOH (0.6 mL, 0.8 mmol) at room temperature overnight. The mixture was concentrated and the residue was redissolved in a mixture of 50% AcOH/H2O (1.4 mL) and MeCN (0.2 mL), filtered and purified by reverse phase preparative HPLC to yield the title compound as a mono-TFA salt (21.2 mg, 99% purity). MS m/z: [M+H]+ calcd for C13H12Cl3NO, 304.00; found 304.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07994209B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-8d4c5d4177814026bd8e1e6398f39400
Quellennotizuspto-grants-2011_08