Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Bromomethyl)-6-phenoxypyridine | HCID 12926387 | — |
| Reactant | HCID 54053742 | HCID 54053742 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53648298 | HCID 53648298 | 83.9% |
Reaction Steps
A solution of trans-5,6-dichloro-1-isopropyl-2-indanol (0.73 g), in anhydrous tetrahydrofuran (7 ml) was added to a suspension of sodium hydride (0.24 g, oil free) in anhydrous tetrahydrofuran (10 ml). The mixture was stirred for 40 minutes and a solution of 2-(bromomethyl)-6-phenoxypyridine (0.84 g) in anhydrous tetrahydrofuran was added, followed by a catalyst amount of tetra-n-butylammonium iodide, The mixture was stirred at room temperature for 18 hours, mixed with water (100 ml) and extracted with diethyl ether (3×50 ml). The combined ether extracts were dried (MgSO4) and condensed under reduced pressure to give an oil which was purified by flash chromatography to give trans-5,6-dichloro-1-isopropyl-2-((6-phenoxypyridin-2-yl)-methoxy)-indane (1.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04666925 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-081427a108bb425d89ab052179a6e01f |
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| Source note | uspto-grants-1987_05 |
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