Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 59583169 | HCID 59583169 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59583113 | HCID 59583113 | 89.7% |
Reaction Steps
An oven-dried 500 mL, 3-neck flask with magnetic stirrer, addition funnel, thermocouple and nitrogen inlet was charged with anhydrous zinc chloride (15.0 g, 0.11 mol) and cooled in an ice/salt bath. 100 mL of THF was then added dropwise. Butyllithium (134 mL, 2.5 M in hexanes, 0.34 mol) was then added dropwise such that the temperature was maintained below 0° C., giving a milky white solution that was stirred at 0° C. for 30 minutes. The ice/salt bath was replaced with a dry ice/acetone bath and the reaction cooled to −75° C. N,N-bis(2,2-dibromovinyl)pyridin-2-amine (5.0 g, 0.011 mol) in 50 mL of THF was added dropwise and the reaction stirred at −75° C. for 20 h. While still at −75° C., 100 mL of 10% acetic acid in THF was added dropwise and the cold solution poured into 150 mL of 1 N HCl. The reaction mixture was extracted with 3×100 mL of ether and the combined organics were washed with 2×100 mL of saturated NaHCO3, dried and evaporated leaving 3.0 g of an colorless liquid as the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586203B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-1aa1cf6087b942a793104060080b0d8e |
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| Source note | uspto-grants-2013_11 |
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