HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Triisopropylsilyl)oxazole-5-carboxaldehyde → HCID 57771144, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Triisopropylsilyl)oxazole-5-carboxaldehyde | HCID 11715805 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Pyridine water | HCID 66926435 | — |
| Product | HCID 57771144 | HCID 57771144 | — |
Reaction Steps
Sodiumboron hydride (200 mg, 5.5 mmol) was added to a solution of 2-triisopropylsilyl-oxazole-5-carboxaldehyde (0.7 g, 2.7 mmol) in a mixture of methanol and tetrahydrofuran (1/1, 20 mL) and the resulting mixture was stirred at room temperature for 20 minutes. The reaction mixture was then diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give (2-triisopropylsilanyl-oxazol-5-yl)-methanol without further purifications. This material was treated with 4-chloro-2-nitro-phenol as described in Preparation 20, Step A, to give 0.7 g of 5-(4-chloro-2-nitro-phenoxymethyl)-2-triisopropylsilanyl-oxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09255110B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-dfb04480f8614d3da80e4d356a7c3cf0 |
| Source note | uspto-grants-2016_02 |