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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42866Generated: October 29, 2026

Nitrogen → HCID 131730012, compound

https://huagongshe.com/reaction/42866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 131730007HCID 131730007—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventPotassium Sodium TartrateHCID 9357—
ProductHCID 131730012HCID 131730012—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-(tert-butyl-dimethyl-silanyloxymethyl)-oxazole-4-carboxylic acid ethyl ester (830 mg, 2.91 mmol) in THF (15.0 mL) was treated at 0° C. with DiBAL (11.6 mL of a 1M sol in toluene, 11.60 mmol) and the reaction mixture was stirred for 45 min at 0° C. The reaction mixture was then diluted with EA (5.0 mL), sat. aq. Rochelle's salt (20.0 mL) was added and the mixture stirred at rt for 2 h. The layers were separated and the aq. layer extracted with EA (3×20 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a yellow solid. TLC: rf (EA)=0.59. LC-MS-conditions 02: tR=0.94 min; [M+H]+=244.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-03425e29addd4b0da28afeb898b6dc6b
Source noteuspto-grants-2013_09