Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Benzyloxy)-4-chloro-2-nitrobenzene | HCID 361282 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15054015 | HCID 15054015 | — |
Reaction Steps
M Vinyl magnesium bromide solution in tetrahydrofuran (80 ml) was added to a stirred solution of 2-benzyloxy-5-chloronitrobenzene (5.28 g, 20 mmol) in tetrahydrofuran (160 ml) at -40° C. The mixture was stirred for 2 hours at -40° C. then poured onto saturated ammonium chloride solution (500 ml) and extracted with ether. The extract was dried and evaporated and the residue was chromatographed on silica in ethyl acetate-hexane (1:8) to give a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281593 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-797e5ce64fbe45e8a94af18b4413e57c |
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| Source note | uspto-grants-1994_01 |
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