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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370505Generated: October 30, 2026

Acetic Anhydride → Lithium Hexamethyldisilazide

https://huagongshe.com/reaction/370505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHexamethyldisilazaneHCID 13838—
Reactant4-Nitrobenzyl 2-(4-allylthioazetidin-2-on-1-yl)acetateHCID 12849631—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventCarbon DisulfideHCID 6348—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductLithium HexamethyldisilazideHCID 2733832—

Reaction Steps

A solution of lithium hexamethyldisilazide was prepared by the addition of 5.12 ml of a 1.6M solution of n-butyllithium in hexane to 1.75 ml of hexamethyldisilazane in 25 ml of dry THF at -10° with stirring, under argon. The solution was cooled to -78° and added by cannula to 1.57 g of 4-nitrobenzyl 2-(4-allylthioazetidin-2-on-1-yl)acetate in 12 ml of dry THF at -78°, with stirring under argon. After 5 minutes 0.846 ml of carbon-disulphide was added by syringe. 1.77 ml of acetic anhydride were then added, followed by 1.07 ml of glacial acetic acid. The solution was allowed to warm to room temperature and evaporated to leave an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526718
Source datasetuspto-grants-1985_07
ORD IDord-c7851fd9a04c48c09e0d20d86bff637a
Source noteuspto-grants-1985_07