HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 23383852, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 23383853 | HCID 23383853 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23383852 | HCID 23383852 | 80% |
Reaction Steps
To a solution of 0.31 mL (3.6 mmol) of oxalyl chloride in 20 mL of CH2Cl2 at −78° C. was added 0.51 mL (7.2 mmol) of DMSO and the reaction mixture was stirred. After 10 min., a solution of 0.49 g (1.8 mmol) of 1-(2,4-dichlorobenzyl)-3-(R)-hydroxymethyl-4-(S)-(3-thienyl)pyrrolidine in 20 mL of CH2Cl2 was then added. After stirring for 10 min. at −78° C., the reaction was allowed to warm to rt. The reaction mixture was poured into ether and extracted twice with sat'd NaHCO3 solution and once with sat'd NaCl solution. The organic fraction was dried over Na2SO4, filtered and the filtrate was concentrated to give 0.49 g of the title compound. Mass Spectrum (ESI) m/e=340 (M+1 35Cl, 35Cl), 342 (M+1 35Cl, 37Cl), and 344 (M+1 37Cl, 37Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455548B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-a3ede8df51d14f4bac01a94798f1e0a2 |
| Source note | uspto-grants-2002_09 |