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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426251Generated: November 3, 2026

Sodium Iodide → tert-Butyl benzyloxy(4-cyanobutyl)carbamate

https://huagongshe.com/reaction/2426251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl N-(benzyloxy)carbamateHCID 736159—
Reactant4-chloropentanenitrileHCID 23266228—
SolventDimethylformamideHCID 6228—
Producttert-Butyl benzyloxy(4-cyanobutyl)carbamateHCID 10685938—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of tert-butyl benzyloxycarbamate in anhydrous dimethylformamide were added 5 mol % of sodium iodide and portionwise 1.36 eq. of sodium hydride (60% dispersion in mineral oil). The mixture was stirred at room temperature for 15 min. before 1.05 eq. of 4-chlorovaleronitrile were added. The mixture was heated to 85° C. and stirred for 3.5 h. After cooling to room temperature the mixture was quenched with water and extracted with diethyl ether. The combined organic phases were concentrated and washed with half saturated aq. sodium thiosulfate, water and brine. The organic phase was dried over sodium sulfate, filtered and concentrated under reduced pressure. The oily residue was washed with petroleum ether and dried under high vacuum to yield Tert-butyl benzyloxy(4-cyanobutyl)carbamate as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968553B2
Source datasetuspto-grants-2011_06
ORD IDord-7353cc4a02e240809d71eedd34a289cb
Source noteuspto-grants-2011_06