Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370506Generated: October 30, 2026

Acetic Anhydride → Lithium Hexamethyldisilazide

https://huagongshe.com/reaction/370506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHexamethyldisilazaneHCID 13838—
Reactant4-Nitrobenzyl 2-(4-allylthioazetidin-2-on-1-yl)acetateHCID 12849631—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventCarbon DisulfideHCID 6348—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductLithium HexamethyldisilazideHCID 2733832—

Reaction Steps

A solution of lithium hexamethyldisilazide was prepared by the addition of 8.66 ml of a 1.6M solution of n-butyllithium in hexane to 2.96 ml of hexamethyldisilazane in 30 ml of dry THF at -10° with stirring under argon. The solution was cooled to -78° and added by cannula to 2.07 g of 4-nitrobenzyl 2-(4-allylthioazetidin-2-on-1-yl)acetate in 15 ml of dry THF at -78°, with stirring, under argon. After 5 minutes 1.11 ml of carbon disulphide were added by syringe. 2.33 ml of acetic anhydride were then added. The solution was allowed to warm to room temperature and evaporated to give an orange oil. The oil was mixed with water (40 ml) and chloroform (40 ml), the organic layer separated and the aqueous layer extracted with additional chloroform (2×40 ml). The combined organic phase was dried (MgSO4) and evaporated to give an orange oil, which was used without further purification as the starting material for Example 16b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526718
Source datasetuspto-grants-1985_07
ORD IDord-31e48194414a48218c9e39db476f0917
Source noteuspto-grants-1985_07