HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 53995682, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Water methylene chloride | HCID 21908982 | — |
| Reactant | HCID 54005021 | HCID 54005021 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53995682 | HCID 53995682 | — |
Reaction Steps
To a solution of 3-[4-(4-trifluoromethylphenoxy)phenoxy]-2-butanone N,N-dimethylhydrazone (5.4 mmol) in THF (15 ml) under nitrogen is added lithium diisopropylamide (6.6 mmol) in THF (15 ml) at 0° for 4 hours. The resulting solution is cooled to -78°, and to it is added ethanal (6.6 mmol). After 1 hour at -78°, the reaction mixture is allowed to warm to 0° and is poured into water/methylene chloride (3:1). The organic phase is separated (3X), and the combined organic extracts are dried over sodium sulfate and concentrated to give 5-hydroxy-2-[4-(4-trifluoromethylphenoxy)phenoxy]-3-hexanone N,N-dimethylhydrazone (cpd. 25, Table C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469872 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-752d70d855aa41b6a1a1ceeea9c871b9 |
| Source note | uspto-grants-1984_09 |