Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamide | HCID 5062348 | — |
| Reactant | HCID 58911280 | HCID 58911280 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58911255 | HCID 58911255 | 99% |
Reaction Steps
In a 200 ml three necked flask fitted with a magnetic stirrer, under inert atmosphere, (4-bromo-2,6-difluoro-phenyl)-pyrrolidin-1-yl-diazene a8 (6.06 g, 0.021 mol.) in THF (50 ml) is added to a solution of diisopropylamide (2 M in THF, 12.5 ml) cooled at −78° C. After 2 h at this temperature, dry DMF (3.2 ml) is added to the green solution. After 1 h, it is poured into water (200 ml), extracted with ether (3×200 ml) and the organic phase is dried over MgSO4, filtered and concentrated in vacuo to give the crude aldehyde a9 (6.62 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244747B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-648ebc66438346ab94ca57c206f1958b |
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| Source note | uspto-grants-2007_07 |
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