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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632257Generated: November 1, 2026

Acetic Anhydride → Lithium Hexamethyldisilazide

https://huagongshe.com/reaction/1632257

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 carbondisulphide 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 numberUS04474793
Source datasetuspto-grants-1984_10
ORD IDord-9436b3a5decf4c2891e8714348ad4a9b
Source noteuspto-grants-1984_10