Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Iodopyrazine | HCID 642841 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14553025 | HCID 14553025 | — |
Reaction Steps
A solution of 2-iodopyrazine (1.0 g, 4.85 mmol) in dry diethylether (10 ml) was added to a solution of n-butyl lithium (4.04 ml of 1.5M, 6.06 mmol) in dry diethylether (20 ml) at -50° C. over a period of 5 minutes under a nitrogen atmosphere. This was followed immediately by the addition of a solution of pivaldehyde (0.65 g, 7.58 mmol) in dry diethylether (10 ml). The reaction mixture was allowed to warm to room temperature over 4 hours and then poured into a mixture of ice and 10% ammonium chloride solution. The aqueous solution was extracted with diethylether (3×50 ml). The combined extracts were washed with water, dried over magnesium sulphate and concentrated under reduced pressure. The residue was taken up in diethylether and filtered through a bed of silica gel. The filtrate was concentrated under reduced pressure to give the product as a clear oil. (0.76 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04975112 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-5ea16f996cc64b7dbd70ccd7f31c6db3 |
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| Source note | uspto-grants-1990_12 |
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