HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 18388380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | [1-Benzyl-4-(trifluoromethyl)pyrrolidin-3-yl]methanol | HCID 18388364 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18388380 | HCID 18388380 | 101.3% |
Reaction Steps
To a solution of 0.98 mL (11.2 mmol) of oxalyl chloride in 30 mL of CH2Cl2 at −78° C. was added 1.6 mL (22.4 mmol) of DMSO and the reaction mixture was stirred for 10 min. To this reaction mixture at −78° C. was added a solution of 1.46 g (5.6 mmol) of 1-benzyl-3-(RS)-hydroxymethyl-4-(RS)-trifluoromethylpyrrolidine in 10 mL of CH2Cl2. After stirring for 10 min. at −78° C., 3.9 mL (28 mmol) of Et3N was added and 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 1.46 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372764B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-f2d7fb9ffb6e4e72a6ae4c0257010dbf |
| Source note | uspto-grants-2002_04 |