HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 86591570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 86591569 | HCID 86591569 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86591570 | HCID 86591570 | 98% |
Reaction Steps
To a solution of methyl 4-[methyl(4-phenyl-2-thiazolyl)aminomethyl]benzoate (2.06 g) in tetrahydrofuran (30 mL) was dropwise added a solution (0.9 M, 30 mL) of diisobutylaluminum hydride in hexane at 0° C. and the mixture was stirred at room temperature for 2 hrs. Diethyl ether was added to the reaction mixture, sodium sulfate 10 hydrate was further added and the mixture was stirred for 2 hrs. After filtering off insoluble materials, the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give white crystals (1.85 g, 98%) of 4-[methyl(4-phenyl-2-thiazolyl)aminomethyl]benzyl alcohol from a fraction eluted with ethyl acetate-hexane (1:1, v/v). melting point: 88-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-793ae9b2979249fd84d1c90d69fbb7f1 |
| Source note | uspto-grants-2007_07 |