HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → N,S-Dimethyl-S-(4-nitrophenyl)sulfoximine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | S-Methyl-S-(4-nitrophenyl)sulfoximine | HCID 12463933 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N,S-Dimethyl-S-(4-nitrophenyl)sulfoximine | HCID 12463940 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
500 mg (2.5 mmol) (RS)—S-(4-nitrophenyl)-S-methylsulfoximide in 4 ml formaldehyde (aqueous, 37%) and 20 ml formic acid (98-100%) are stirred in the open flask at 100° C. After 22 hours, the solvent is evaporated, the mixture is treated again with 4 ml formaldehyde (aqueous, 37%) and 20 ml formic acid (98-100%) and stirred for a further 22 hours at 100° C. Residues of the solvent are removed on the rotary evaporator. The remaining residue is dissolved with 2N HCl and extracted with dichloromethane. The aqueous phase is basified with NaHCO3 and extracted with dichloromethane. The combined organic phases are dried (Na2SO4), filtered and concentrated. 448 mg (2.1 mmol, corresponding to 85% of theor.) of the product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524724B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-8d6326d28bb84f0f8b5f7f7838b8aadd |
| Source note | uspto-grants-2013_09 |