HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → (Methyl(trityl)amino)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 566949-46-0 | HCID 5080555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Methyl(trityl)amino)acetaldehyde | HCID 85849001 | — |
Reaction Steps
A solution of DMSO (1.47 mL, 20.8 mmol) in 60 mL of CH2Cl2 was cooled to −78° C. and treated with oxalyl chloride dropwise under N2 atmosphere for 10 min. The resulting mixture was treated with a solution of 2-[methyl(trityl)amino]ethanol (3.0 g, 9.45 mmol) in 10 mL of CH2Cl2 dropwise and stirred for additional 15 min. Triethylamine (6.6 mL, 47.3 mmole) was added to the mixture and warmed up to room temperature. The reaction was quenched by adding water and diluted with 100 mL of CH2Cl2. The organic phase was washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was triturated with ether to give the product as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852731B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-56ccc7f70d6443868d0e1b72742fc30d |
| Source note | uspto-grants-2005_02 |