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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612765Generated: November 1, 2026

Acetic Acid → HCID 9996173, compound

https://huagongshe.com/reaction/1612765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN-Boc-glycine methyl esterHCID 637609—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 10352026HCID 10352026—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9996173HCID 9996173—

Reaction Steps

A solution of 5.82 g of lithium diisopropylamide in 30 ml of anhydrous tetrahydrofuran is cooled to -78° C. under an inert atmosphere. Under constant stirring at -78° a solution of 9.84 g of ethyl n-butyl(methyl)phosphinate in 20 ml of anhydrous tetrahydrofuran is added over 15 minutes under a positive pressure of an inert atmosphere via a canula. The resulting pale yellow solution is stirred for 1 hour at -78° and a pre-cooled (-78° C.) solution of 1.89 g of N-tert.-butoxycarbonylglycine methyl ester in 10 ml of anhydrous tetrahydrofuran is added over 5 minutes via a canula. Thin layer chromatography indicates complete reaction after circa 10 minutes. At -78° 4.0 g of glacial acetic acid is added and the mixture is allowed to warm to room temperature. The reaction mixture is diluted with dichloromethane and washed with water. Drying over magnesium sulphate and removal of the solvent in vacuo affords a pale yellow oil. Removal of the excess starting material by distillation and chromatography of the resulting yellow oil on silica gel yields ethyl 3-(N-tert.-butoxycarbonylamino)-2-oxo-propyl(n-butyl)phosphinate as a colourless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190934
Source datasetuspto-grants-1993_03
ORD IDord-afca730c5cd040d9baf56774e3025fc9
Source noteuspto-grants-1993_03