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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756883Generated: October 28, 2026

Phosphate → HCID 131719087, compound

https://huagongshe.com/reaction/1756883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiphenylphosphinic chlorideHCID 73910—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 10326224HCID 10326224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131719087HCID 13171908795.8%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A solution of 1.2 g of 3-{(2R)-2-[(3S, 4R)-1-allyloxycarbonylmethyl-3-[(1R )-1-t-butyldimethylsilyloxyethyl]-2-oxoazetidin-4-yl]propionyl}-spiro[2,3-dihydro-4H-1,3-benzoxazine-2,1'-cyclohexan]-4-one in 6 ml of tetrahydrofuran is added dropwise to 4.4 ml of 1M sodium bis(trimethylsilyl)amide solution (solvent:tetrahydrofuran) at a temperature from -20° C. to -30° C. during one minute. 261 mg of trimethylsilyl chloride are added thereto at -50° C. and the mixture is stirred for 2 minutes. Then, 645 mg of diphenylphosphoryl chloride are added thereto at -50 ° C. and the mixture is stirred for 2 hours at 0° C. The reaction mixture is poured into 50 ml of 0.2M phosphate buffer (pH 7.0) and the mixture is extracted with ethyl acetate. The extract is washed, dried and evaporated to remove the solvent. Isopropyl ether is added to the residue and the resulting precipitates of 355 mg of spiro[2,3-dihydro-4H-1,3-benzoxazine-2,1'-cyclohexan]-4-one are removed by filtration. The filtrate is condensed to obtain 1.04 g of (1R, 5R, 6S)-6-[(1R)-1-t-butyldimethylsilyloxyethyl]-1-methyl-2-diphenylphosphoryloxy-carbapen-2-em-3-carboxylic acid.allyl ester as syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442055
Source datasetuspto-grants-1995_08
ORD IDord-11e8e332b8e147bc9741d5ab83ca6c89
Source noteuspto-grants-1995_08