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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2-phenylanilineHCID 229550—
Reactanttert-Butyl 3-ButenoateHCID 639778—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Producttert-butyl (3E)-4-(3-amino-4-phenylphenyl)-3-butenoateHCID 6659745378.8%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072734B2
Source datasetuspto-grants-2015_07
ORD IDord-cb84ccb8ef9742119fd83111ef388a03
Source noteuspto-grants-2015_07