HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylamine → HCID 20253724, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 20253690 | HCID 20253690 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20253724 | HCID 20253724 | 64.3% |
Reaction Steps
A solution of 0.42 g of approximately 85% pure m-chloroperoxybenzoic acid in 90 ml of methylene chloride is added dropwise to a solution of 0.9 g of 6-chloro-6,7,7-trifluoro-6,7-dihydro-2-[(4-methoxy-3-methyl-2-pyridyl)methylthio]-1H-[1,4]-dioxino[2,3-f]benzimidazole in 180 ml of methylene chloride at -40° C., with stirring. Stirring is continued for 4 hours and the solution is allowed to come to -20° C. 0.29 ml of trimethyl amine are added, and the organic phase is washed with potassium bicarbonate solution and with water, dried with magnesium sulfate and concentrated in vacuo. The residue is stirred with ethyl acetate and subsequently with acetone. 0.6 g (64%) of the title compound of m.p. 198°-200° C. (decomposition) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560693 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-3d9d4f874d134c3490977f46afb81791 |
| Source note | uspto-grants-1985_12 |