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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1852060Erstellt: 26. Oktober 2026

Triethylamine → (E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acryloyl azide

https://huagongshe.com/reaction/1852060

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt(E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acrylic acidHCID 5343159—
LösungsmittelBenzeneHCID 241—
Produkt(E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acryloyl azideHCID 8668317084,5%

Reaktionsschritte

(E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acrylic acid (5 g, 24.25 mmol), diphenylphosphoryl azide (4.96 mL, 23.04 mmol), and Et3N (6.76 mL, 48.5 mmol) were dissolved in benzene and stirred for 16 h. The solution was concentrated under vacuum and the residue was purified by silica gel chromatography using 20% EtOAc/Hexanes to give 4.5 g of (E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acryloyl azide as a yellow solid, which was taken into PhCH2Ph (50 mL). The resulting solution was slowly heated to 80° C. for 1 h and then to reflux for 3 h. After cooling to rt, the solid was collected washing with benzene to give 3.5 g of the desired product 2,3-dihydro-[1,4]dioxino[2,3-f]isoquinolin-7-ol as a solid. 1H NMR (400 MHz, CD3OD) δ ppm 4.37 (m, 4H), 6.83 (d, J=7.09 Hz, 1H), 7.02 (d, J=8.80 Hz, 1H), 7.12 (d, J=7.34 Hz, 1H), 7.79 (d, J=8.80 Hz, 1H); MS: (M+H)+ 204.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08957203B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-f4bfd13f1eab46d4a6d799a38b10c652
Quellennotizuspto-grants-2015_02