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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044744Generated: October 30, 2026

Nitrogen → HCID 86649487, compound

https://huagongshe.com/reaction/1044744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazoleHCID 66821548—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86649487HCID 86649487—

Reaction Conditions

Temperature-40 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 2-[1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-oxazole (733 mg, 3.22 mmol) in dry THF (16 mL) was added tert-BuLi (2.62 mL of a 1.6 M solution in pentane, 4.19 mmol) at −78° C. The reaction mixture was then stirred for 1 h at −40° C. and cooled to −78° C. before N,N-dimethylformamide (0.49 mL, 6.44 mmol) was added dropwise. The reaction mixture was allowed to warm up to rt over a period of 1 h and stirred at this temperature for 2 h. Water (30 mL) and sat. aq. NH4Cl (20 mL) were added, the layers separated and the aq. layer extracted with EA (2×30 mL). The combined org. extracts were dried over MgSO4, filtered, 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)=0.33. LC-MS-conditions 02: tR=1.08 min; [M+H]+=256.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-7bc31a00e8364d9c96fb5b778582560b
Source noteuspto-grants-2013_10