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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | (E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acrylic acid | HCID 5343159 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acryloyl azide | HCID 86683170 | 84.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957203B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f4bfd13f1eab46d4a6d799a38b10c652 |
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| Source note | uspto-grants-2015_02 |
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