HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 4-Chloromethyl-thiazole-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | [4-(Chloromethyl)-1,3-thiazol-2-yl]methanol | HCID 11073749 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | 2-Oxopropiononitrile | HCID 69430 | — |
| Product | 4-Chloromethyl-thiazole-2-carbaldehyde | HCID 55298544 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (4-chloromethyl-thiazol-2-yl)-methanol (1.60 g, 9.80 mmol) in AcCN (98.0 mL) was treated at rt with MnO2 (4.73 g, 49.01 mmol). The reaction mixture was stirred at rt overnight before being filtered through Celite and the solvent was removed under reduced pressure. Purification of the residue by FC (4:1 hept-EA) gave the title compound as a colorless oil. TLC:rf (4:1 hept-EA)=0.37. LC-MS-conditions 02: tR=0.77 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536209B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-7a7c569c4fa34f09b0e58e1a59c58918 |
| Source note | uspto-grants-2013_09 |