HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-5-nitroindan-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-((Tert-butyldimethylsilyl)oxy)acetaldehyde | HCID 4187788 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 5-Nitro-2,3-dihydro-1H-inden-2-amine sulfate | HCID 16083811 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-5-nitroindan-2-amine | HCID 58289869 | 64% |
Reaction Steps
0.91 g of sodium cyanoborohydride was added to a methanol (100 mL) solution of 2 g of 5-nitroindan-2-amine sulfate and 1.9 g of (tert-butyldimethylsiloxy)acetaldehyde, and stirred at room temperature for 2 days. The reaction liquid was neutralized with aqueous saturated sodium bicarbonate solution, and methanol was evaporated away under reduced pressure. The residue was diluted with water, and extracted three times with chloroform. The organic layer was dried with anhydrous magnesium sulfate, the solvent was evaporated away under reduced pressure, and the crude product was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain 1.56 g of the entitled compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436004B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-d56af1afab2046bb97dec5633142f664 |
| Source note | uspto-grants-2013_05 |