HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179400Generated: October 26, 2026
Sodium Azide → 2-(2-Azidoethyl)-5-bromo-7-chlorobenzofuran
https://huagongshe.com/reaction/2179400
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-(5-Bromo-7-chlorobenzofuran-2-yl)ethyl 4-methylbenzenesulfonate | HCID 86668003 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Azidoethyl)-5-bromo-7-chlorobenzofuran | HCID 86668004 | 75% |
Reaction Steps
To a solution of the product of step C (2.3 g, 5.35 mmol) in dimethylformamide (11 mL) was added sodium azide (1.2 g, 18.73 mmol) at ambient temperature. The reaction mixture was heated at 70° C. for 2 h, cooled and quenched with water then extracted with ethyl acetate (2×15 mL). The combined organic extracts were dried over Na2SO4 and concentrated in vacuo to give the crude product which was purified by column chromatography (SiO2, 4:1 hexanes/ethyl acetate) providing 2-(2-azidoethyl)-5-bromo-7-chlorobenzofuran (1.2 g, 75%) as an off-white solid: 1H NMR (CDCl3, 400 MHz) δ 7.52-7.49 (m, 1H), 7.37-7.35 (m, 1H), 6.50 (s, 1H), 3.67 (t, J=6.8 Hz, 2H), 3.07 (t, J=6.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067949B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f7b1bc037543499a923c143918cd1abf |
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| Source note | uspto-grants-2015_06 |
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