Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 18327737 | HCID 18327737 | — |
| Product | HCID 10198149 | HCID 10198149 | 93.3% |
Reaction Steps
A solution of (4E)-N-methyl-N-(tert-butoxycarbonyl)-5-(3-amino-4-methylphenyl)-4-penten-2-amine (1.50 g, 4.93 mmol) and aqueous hydrobromic acid (50%, 25 mL) was stirred at 0° C. to ambient temperature for ˜16 h. The reaction mixture was extracted with chloroform (40 mL). The aqueous layer was cooled to 0° C. and basified with aqueous sodium hydroxide solution to pH 8-9 and extracted with chloroform (3×50 mL). The combined extracts were dried over sodium sulfate, filtered and concentrated on a rotary evaporator to yield 0.938 g (93.3%) of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06337351B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-9b0afa5be8a24d09be88558af0d8cb39 |
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| Source note | uspto-grants-2002_01 |
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