Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 23000604 | HCID 23000604 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59085849 | HCID 59085849 | — |
Reaction Steps
To a solution of 1.15 g (3.16 mmol) of 2-[2-({[(benzyloxy)carbonyl]amino}methyl)phenyl]ethyl methanesulfonate in 8.0 mL of DMF was added 0.411 g (6.33 mmol) of sodium azide. After stirring at room temperature overnight, an additional 0.205 g (3.15 mmol) of sodium azide was added and the reaction warmed to 40° C. for 4 h. The reaction was cooled to room temperature, treated with saturated sodium carbonate (aq) and extracted with ethyl acetate (3×). The organic extracts were combined, washed with water (1×) and brine (1×), dried over sodium sulfate and concentrated to dryness in vacuo to give 1.2 g of a crude oil. Flash chromatography on silica gel (20% ethyl acetate in hexane) gave benzyl 2-(2-azidoethyl)benzylcarbamate as a colorless oil: 1H NMR (CDCl3, 400 MHz): δ 7.39-7.20 (m, 9H), 5.14 (s, 2H), 5.05 (br s, 1H), 4.42 (d, 2H, J=5.6 Hz), 3.56-3.49 (t, 2H, J=7.0 Hz), 2.97-2.91 (t, 2H, J=7.0 Hz); MS (Electrospray): M+Na=333.1; TLC Rf=0.32 (20% ethyl acetate in hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515011B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-16bfee0177784be5b491a84c53be2321 |
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| Source note | uspto-grants-2003_02 |
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