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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52806Generated: October 26, 2026

Imidazole → N-[(Phenylmethoxy)carbonyl]-O-[(1,1-dimethylethyl)dimethlsilyl]-L-homoserine

https://huagongshe.com/reaction/52806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantMethanolHCID 887—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantCbz-L-HomoserineHCID 489187—
SolventDimethylformamideHCID 6228—
ProductN-[(Phenylmethoxy)carbonyl]-O-[(1,1-dimethylethyl)dimethlsilyl]-L-homoserineHCID 54368725—

Reaction Steps

[(1,1-Dimethylethyl)dimethylsilyl]chloride (37.5 g., 249 mmol.) was added to a solution of N-[(phenylmethoxy)carbonyl]-L-homoserine [prepared as described in Example 6(a), 41.56 mmol.] in dimethylformamide (125 ml.), followed by imidazole (33.95 g., 498 mmol.). The resulting light yellow solution was stirred at room temperature for 22 hours. Methanol (500 ml.) was added, the reaction mixture was stirred for an additional 6 hours, and then the methanol and most of the dimethylformamide were removed in vacuo. The remaining residue was taken up into ethyl acetate (800 ml.), washed with 10% citric acid (2×300 ml.), and the combined aqueous phase was extracted with ethyl acetate (300 ml.). The combined ethyl acetate phase was washed with water and brine, dried (sodium sulfate), concentrated, and the residue was evaporated with hexane to form a white powder. This powder was dried in vacuo to give 12.942 g. of title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616775
Source datasetuspto-grants-1997_04
ORD IDord-0fc771a71c974358a5f5b9a640a2e38f
Source noteuspto-grants-1997_04