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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42823Generated: October 29, 2026

Nitrogen → HCID 131730004, compound

https://huagongshe.com/reaction/42823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
ReactantHCID 131730005HCID 131730005—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 131730004HCID 131730004—

Reaction Conditions

Temperature-50 °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-bromo-5-(tert-butyl-dimethyl-silanyloxymethyl)-thiazole (3.00 g, 9.73 mmol) in dry Et2O (20 mL) was added to a n-BuLi (4.30 mL of a 2.5M solution in hexanes, 10.70 mmol) solution in Et2O (50 mL) at −78° C. The reaction mixture was then stirred for 40 min at −78° C. before N,N-dimethylacetamide (1.81 mL, 19.46 mmol) was added dropwise. The reaction mixture was allowed to warm up to −50° C. and stirred at this temperature for 20 min. Sat. aq. NH4Cl (20 mL) was added, the layers separated and the aq. layer extracted with Et2O (3×20 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure to give the title compound as a yellow oil. TLC:rf (1:2 hept-EA)=0.80. LC-MS-conditions 01: tR=1.09 min, [M+1-1]+=271.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-54d4bf19511c4b658be754d798ec37db
Source noteuspto-grants-2013_09