HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyraldehyde → HCID 59625522, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 4-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate | HCID 59625163 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 59625522 | HCID 59625522 | 91.3% |
Reaction Steps
To a solution of tert-butyl 4-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate (840 mg) and 2-methylpropanal (256 mg) in dichloroethane (10 ml) were added acetic acid (203 mg) and sodium triacetoxyborohydride (931 mg). The mixture was stirred at room temperature for 1 hr. The mixture was neutralized with 6% aqueous sodium hydrogen carbonate. After partitioning, the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and the fraction eluted with ethyl acetate-hexane (1:1) was concentrated under reduced pressure to give the object compound (940 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329691B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-4ca9ab7fa22c42a884ea2157dba8e4ec |
| Source note | uspto-grants-2012_12 |