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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773584Generated: November 1, 2026

2-(Triisopropylsilyl)oxazole-5-carboxaldehyde → HCID 57771144, compound

https://huagongshe.com/reaction/1773584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Triisopropylsilyl)oxazole-5-carboxaldehydeHCID 11715805—
ReactantHCID 178418435HCID 178418435—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventPyridine waterHCID 66926435—
ProductHCID 57771144HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-dfb04480f8614d3da80e4d356a7c3cf0
Source noteuspto-grants-2016_02