HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 3-(2-Ethylbutyl)cyclobutanecarbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | N-Methoxy-N-methyl-3-(2-ethylbutyl)cyclobutanecarboxamide | HCID 86675050 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Ethylbutyl)cyclobutanecarbaldehyde | HCID 86675051 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of N-methoxy-N-methyl-3-(2-ethylbutyl)cyclobutanecarboxamide (13.2 g) in methylene chloride (35 mL) was added dropwise diisobutylaluminum hydride (1.0 M in methylene chloride)(76.0 mL) at −78° C. After stirring at −78° C. for 2.5 hr, 1 M sulfuric acid was added dropwise to the mixture. The mixture was stirred at ice temperature for 20 min. The organic layer was removed, and the aqueous layer was extracted with methylene chloride (15 mL×2). The combined organic layer was washed with 0.5 N sulfuric acid (50 mL×2), water (50 mL) and brine, then dried over sodium sulfate. The sodium sulfate was filtered off and the filtrate comprising the title compound was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604069B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-73f7336ad9424a50a23573efe4aa2199 |
| Source note | uspto-grants-2013_12 |