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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975459Generated: October 30, 2026

Ethyl Acetate → 2-(N-allyloxycarbonylaminomethyl)-3-(t-butyldimethylsilyloxy)butylamine

https://huagongshe.com/reaction/1975459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant2-(N-allyloxycarbonylaminomethyl)-3-t-butyldimethylsilyloxy-1-methanesulfonyloxybutaneHCID 19099292—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(N-allyloxycarbonylaminomethyl)-3-(t-butyldimethylsilyloxy)butylamineHCID 19099316202.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 7.00 g of 2-(N-allyloxycarbonylaminomethyl)-3-t-butyldimethylsilyloxy-1-methanesulfonyloxybutane and 1.42 g of ammonium chloride in 70 ml of N,N-dimethylformamide was added 1.73 g of sodium azide at 0° C. The mixture was stirred at 50° C. for 7 hours. After the starting material disappeared, 350 ml of ethyl acetate and 350 ml of water were added to the reaction mixture. The organic layer was washed in turn with water three times and brine. The half amount of solvent was evaporated and then 5.11 g of triphenylphosphine was added thereto portionwise. After stirring overnight, 2.15 g of 28% aqueous ammonia was added and the mixture was stirred for 8 hours, and then evaporated under reduced pressure to give 11.36 g of crude 2-(N-allyloxycarbonylaminomethyl)-3-(t-butyldimethylsilyloxy)butylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286721
Source datasetuspto-grants-1994_02
ORD IDord-be3f58fd5d2448d9b1fe5f886841c916
Source noteuspto-grants-1994_02