HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554414Generated: October 31, 2026
Sodium borohydride → HCID 66925240, compound
https://huagongshe.com/reaction/554414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Reactant | HCID 86232871 | HCID 86232871 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66925240 | HCID 66925240 | 87% |
Reaction Steps
4,5-Diphenyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (202 mg) was dissolved in methanol (2 mL) and tetrahydrofuran (2 mL), 40% methylamine methanol solution (0.5 mL) was added at room temperature, and the mixture was stirred for 15 min. To the reaction mixture was added sodium borohydride (22 mg) at room temperature, and the mixture stirred for 1 hr. The reaction mixture was concentrated under reduced pressure, to the residue was added saturated aqueous sodium hydrogencarbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: ethyl acetate) to give the title compound as white crystals (yield 181 mg, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08048909B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-89f0b32de6ad4ac98c4547cde9e3811f |
|---|
| Source note | uspto-grants-2011_11 |
|---|