HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518632Generated: November 4, 2026
Tri-o-tolylphosphine → tert-butyl (3E)-4-(3-amino-4-phenylphenyl)-3-butenoate
https://huagongshe.com/reaction/1518632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-2-phenylaniline | HCID 229550 | — |
| Reactant | tert-Butyl 3-Butenoate | HCID 639778 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl (3E)-4-(3-amino-4-phenylphenyl)-3-butenoate | HCID 66597453 | 78.8% |
Reaction Steps
2-Phenyl-4-bromoaniline (564.7 mg, 2.28 mmol) was dissolved in N,N-dimethylformamide (25 mL) and, at room temperature, thereto were added tert-butyl-3-butenoate (582.5 mg, 4.10 mmol), tri-(o-tolyl)phosphine (1.87 g, 6.16 mmol), and diisopropylethylamine (0.78 mL, 4.56 mmol). The reaction mixture was deaerated, palladium acetate (67.4 mg, 0.30 mmol) was added, and the mixture was deaerated again. After stirring at 90° C. overnight, the reaction mixture was filtered through celite and washed with ethyl acetate (120 mL). The organic layer was washed with a saturated aqueous solution of sodium chloride (50 mL), thereafter dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by a silica gel column to obtain tert-butyl (3E)-4-(3-amino-4-phenylphenyl)-3-butenoate (555.8 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09072734B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-cb84ccb8ef9742119fd83111ef388a03 |
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| Source note | uspto-grants-2015_07 |
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