HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Methylthio)benzaldehyde → HCID 69055255, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Methylthio)benzaldehyde | HCID 76985 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Aminobutyric acid methyl ester hydrochloride | HCID 2756383 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69055255 | HCID 69055255 | 105.7% |
Reaction Steps
3 g of methyl 4-aminobutyrate hydrochloride and 2.8 ml of triethylamine were added to a chloroform solution of 2 g of 4-(methylthio)benzaldehyde, and 8.4 g of sodium triacetoxyborohydride was added to it, and stirred overnight. Aqueous sodium hydrogencarbonate solution was added to it, extracted with chloroform, and the organic layer was washed with saturated saline water. This was dried with anhydrous sodium sulfate, the solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography to obtain 2.88 g of 1-[4-(methylthio)phenyl]pyrrolidin-2-one as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338460B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-195a127fe3a8465e9791bd550e2149b1 |
| Source note | uspto-grants-2012_12 |