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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852060Generated: October 25, 2026

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

https://huagongshe.com/reaction/1852060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acrylic acidHCID 5343159—
SolventBenzeneHCID 241—
Product(E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acryloyl azideHCID 8668317084.5%

Reaction Steps

(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957203B2
Source datasetuspto-grants-2015_02
ORD IDord-f4bfd13f1eab46d4a6d799a38b10c652
Source noteuspto-grants-2015_02