HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → HCID 20690187, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,1,1-Trifluoro-N-(2-methoxyethyl)methanesulfonamide | HCID 20571257 | — |
| Product | HCID 20690187 | HCID 20690187 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Oxalyl chloride (1.27 grams; 0.01 mole) is added portionwise to a stirred solution of N-(2-methoxyethyl)trifluoromethanesulfonamide (4.0 grams; 0.02 mole) and triethylamine (2.0 grams; 0.02 mole) in 1,2-dimethoxyethane (40 mls) at 0° C. under a nitrogen atmosphere. After the addition is completed, the reaction mixture is stirred at 0° C. for one hour, heated to 50° C. and stirred thereat for 2 hours, and concentrated to remove the solvent. The residue is then extracted with diethyl ether and the ether extract is evaporated to obtain 4.65 grams (99% of theoretical) of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226738 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-8d48518e5e9446b5b81fa8a5a81df680 |
| Source note | uspto-grants-1980_10 |