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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256329Generated: October 31, 2026

Water → HCID 178484874, compound

https://huagongshe.com/reaction/256329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 67852048HCID 67852048—
ReactantHCID 178486001HCID 178486001—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178484874HCID 178484874—

Reaction Steps

23.1 g (0.03 mole) of N-benzyloxycarbonyl-N-methyl-D-phenylalanyl-L-prolyl-Nω -benzyloxycarbonyl-L-arginine-aldehyde (Example 1, Step 2) are dissolved in 150 ml of ethanol, 50 ml of deionized water and 48 ml of N sulfuric acid are added and the mixture is submitted to hydrogenolysis in the presence of 3 g of a 10 percent Pd/C catalyst. The progress of the hydrogenolysis is monitored by thin-layer chromatography in a developing solvent of ethyl acetate-pyridine-acetic acid-water-30:20:6:11 (Rf values of the starting material, intermediary and final product about 0.9, 0.7 and 0.4, respectively). After completed reaction the catalyst is filtered and washed three times with 30 ml of deionized water. The filtrate and washings are combined and concentrated to about 100 ml in a rotary evaporator. The aqueous residue is diluted to about 200 ml with deionized water and its pH is controlled. If it is not between 6.0 and 6.5, it is adjusted with 0.1N sulfuric acid or an ion-exchange resin in OH cycle (i.e. AG 1X8), then the solution is freeze-dried. Yield 12.4 g (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703036
Source datasetuspto-grants-1987_10
ORD IDord-f2b95549444d4614b2afc23aaa5fd4b7
Source noteuspto-grants-1987_10