Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 18448592 | HCID 18448592 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18448589 | HCID 18448589 | — |
Reaction Steps
4-Chloro-7-cyanochroman (Step C) (8.1 g, 42 mmol) was dissolved in dry DMF (90 mL) and NaN3 (4.0 g, 62 mmol) was added and the reaction was heated to 80° C. under N2. After 5 h TLC (SiO2, toluene) showed that no starting chloride was present. The reaction was cooled and partitioned between EtOAc (200 mL) and H2O (150 mL). The organic phase was washed with H2O (2×100 mL) and brine (100 mL). The solution was dried over MgSO4, filtered and concentrated in vacuo to provide a residue which was purified by column chromatography (SiO2, 15% EtOAc in hexane) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425631B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-98fd8387528a469cbcf5e2db00cdee14 |
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| Source note | uspto-grants-2008_09 |
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