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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372599Generated: October 31, 2026

Phosphoric Acid → HCID 13132322, compound

https://huagongshe.com/reaction/2372599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantSodium AcetateHCID 517045—
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13132297HCID 13132297—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 13132322HCID 1313232226.9%

Reaction Steps

Nε -Carbobenzoxy-L-lysyl-N-(indan-2-yl)glycine tert-butyl ester oxalate (3.5 g) is dissolved in 20 ml of methanol, and 1 g of sodium acetate, 1.2 g of acetic acid, 8 g of molecular sieve and 15 g of ethyl 2-oxo-4-phenyl-butyrate are added. To this mixture is added dropwise with stirring a solution of 3.3 g of sodium cyanoborohydride in 30 ml of methanol over 2 hours. 3 g of sodium cyanoborohydride is further added, and the mixture is stirred for 3 hours. After addition of 200 ml of 25% aqueous phosphoric acid, the reaction mixture is extracted with two 200-ml portions of ethyl acetate. The extract is washed with 0.5 N aqueous sodium hydroxide and with water, and dried over anhydrous magnesium sulfate. The ethyl acetate is distilled off under reduced pressure, and the oil thus obtained is separated and purified by silica gel column chromatography (acetone-benzene (1:12 to 1:5). The first fraction gives 1.1 g of Nα -[1-(R)-ethoxycarbonyl-3-phenylpropyl]-Nε -carbobenzoxy-L-lysyl-N-(indan-2-yl)glycine tert-butyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05098892
Source datasetuspto-grants-1992_03
ORD IDord-59aebc5442de4be4a0015aa08d3bb15e
Source noteuspto-grants-1992_03