HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235487Generated: October 30, 2026
Benzophenone imine → HCID 86049192, compound
https://huagongshe.com/reaction/2235487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2-Chloro-N,N-dipropylpyridin-4-amine | HCID 86049190 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86049192 | HCID 86049192 | 75.8% |
Reaction Steps
A mixture of 0.52 g (2.4 mmol) of 2-chloro-N4,N4-dipropylpyridin-4-amine, 0.076 g (0.12 mmol) of racemic 2,2′-bis(diphenylphosphino)-1,1′-binaphtyl (BINAP), 0.33 g (3.4 mmol) of sodium tert-butoxide and 0.027 g (0.12 mmol) of palladium (II) acetate in 25 mL of toluene was treated with 0.49 mL (2.9 mmol) of benzophenone imine and heated to 85° C. for 18 h. The crude reaction mixture was diluted with ethyl acetate, filtered through a pad of celite and purified by flash chromatography eluting with a 33% hexanes/ethyl acetate mixture to give 0.65 g (75%) of the title compound as a golden oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714009B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-73a1e29d9ee54c14b2e7871e28984719 |
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| Source note | uspto-grants-2010_05 |
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