Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Bromo-4-methoxy-6-nitrophenol | HCID 11265140 | — |
| Reactant | HCID 101645068 | HCID 101645068 | — |
| Catalyst | Manganese | HCID 23930 | — |
| Catalyst | chromium(II) dichloride | HCID 10197677 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22144525 | HCID 22144525 | — |
Reaction Steps
tert-Butyl-chloro-silane (0.25 ml) was added to a mixture of 2-bromo-4-methoxy-6-nitro-phenol (0.124 g), chromium (II) chloride (0.012 g) and manganese (0) powder (0.137 g) in dimethylformamide (3 mL). The mixture was subjected to microwaves for 4 min at 150° C. Benzaldehyde (0.06 mL) was added and the reaction was subjected to microwaves for 6 min at 150° C. Water (0.5 mL) was added, then after 30 min the mixture was filtered through a pad of celite. The above procedure was repeated three more times. The combined filtrate was partitioned between dilute aq. HCl (100 mL) and ethyl acetate (100 mL). The organic layer was dried over sodium sulfate, filtered through celite and concentrated. Chromatography on silica gel (eluant: gradient 0 to 30% ethyl acetate:hexane) afforded 7-bromo-5-methoxy-2-phenyl-benzooxazole (0.13 g). MS: 304 (95%), 306.4 (100%) (MH+); HPLC tR: 2.79 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045539B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-e61e9eb7c38d49e893c5dae203141b77 |
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| Source note | uspto-grants-2006_05 |
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