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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167292Generated: November 2, 2026

Hexamethyldisilazane → HCID 58506468, compound

https://huagongshe.com/reaction/2167292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 79244—
ReactantHCID 13818179HCID 13818179—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58506468HCID 5850646874%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a solution of hexamethyldisilazane (17.5 g, 106 mmol) in THF (100 mL) was added n-butyllithium (1.58 M in hexane, 50 mL, 78.5 mmol) at −78° C. After 5 min at −78° C., the solution was allowed to warm to 0° C. for 30 min and then cooled to −78° C. again. A solution of 3-benzoyl-4-methyl-2-phenyl-1,3-oxazolidin-5-one (dried overnight in vacuo before using, 20 g, 71 mmol) in THF (250 mL) was added slowly under argon, and the dark red brown solution was stirred at this temperature for 3 h. A solution of N-(bromomethyl)phthalimide (22.2 g, 92.5 mmol) in THF (200 mL) was then added dropwise. The reaction mixture was allowed to warm to 20° C. in 4 h and stirred at this temperature overnight. The solvent was evaporated. The residue was dissolved in 10% NH4Cl (250 mL) and extracted with CH2Cl2. The organic phase was dried over Na2SO4 and evaporated. Recrystallization from CH2Cl2 and ether (1:4) gave white crystals of 2-((3-benzoyl-4-methyl-5-oxo-2-phenyloxazolidin-4-yl)methyl)isoindoline-1,3-dione (23 g, 74%). LC-MS (ES, m/z): 441 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045440B2
Source datasetuspto-grants-2015_06
ORD IDord-1f89f56c2d1b4abbbd61a02ea3eadf47
Source noteuspto-grants-2015_06