Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 18327736 | HCID 18327736 | — |
| Product | HCID 10198785 | HCID 10198785 | 99.8% |
Reaction Steps
A solution of (4E)-N-methyl-N-(tert-butoxycarbonyl)-5-(3-acetamido-4-methylphenyl)-4-penten-2-amine (0.90 g, 2.60 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., basified with aqueous sodium hydroxide solution to pH 8-9, and extracted with chloroform (4×50 mL). The combined extracts were dried over sodium sulfate, filtered and concentrated on a rotary evaporator to yield 0.639 g (94.6%) of a colorless 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-af96af9ae0eb4e669f03283ce09a8212 |
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| Source note | uspto-grants-2002_01 |
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