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HRID 1172215Erstellt: 26. Oktober 2026

Ammonium Chloride → diazo-(3,4-Difluoro-phenyl)acetic acid allyl ester

https://huagongshe.com/reaction/1172215

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt4-Acetamidobenzenesulfonyl azideHCID 5129185—
Edukt(3,4-Difluoro-phenyl)acetic acid allyl esterHCID 67422777—
LösungsmittelAcetonitrileHCID 6342—
Produktdiazo-(3,4-Difluoro-phenyl)acetic acid allyl esterHCID 8660958697,4%

Reaktionsschritte

(3,4-Difluoro-phenyl)acetic acid allyl ester (64 g) was dissolved in acetonitrile (400 mL) and 4-acetamidobenzenesulfonyl azide (p-ABSA, 87 g, 0.36 mol) was added and the mixture stirred at room temperature for 15 min. The mixture was then cooled to 0° C. and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 58.6 mL) was added dropwise at 0° C. during 30 min. The mixture was allowed to warm up to rt (room temperature) and stirred at rt for 4-20 h (until TLC showed completion of reaction). Saturated ammonium chloride (500 mL) was added and the organic phase was separated from the water phase. The water phase was extracted with diethylether (3×200 mL) and the four combined organic phases were dried (Magnesium sulphate) and evaporated in vacuo. The resulting solid was extracted with a 50:50 mixture of diethylether/pentane (3×200 mL). The combined ether phases were evaporated in vacuo (keep temperature below 40°) and purified by flash column chromatography (silicagel, eluent: 10:90 mixture of diethylether/pentane). The yellow fractions were combined and evaporated in vacuo (keep temperature below 40°) to give 70 g diazo-(3,4-Difluoro-phenyl)acetic acid allyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07834008B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-c65d640cd3e24958a8ab4b938cf6e4bc
Quellennotizuspto-grants-2010_11