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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790780Generated: October 29, 2026

Hydrochloric Acid → HCID 23387363, compound

https://huagongshe.com/reaction/1790780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 86585845HCID 86585845—
CatalystTetrabutylammonium BromideHCID 74236—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 23387363HCID 23387363—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 3-buten-1-yl-3-(N-benzyloxycarbonyl-L-valyloxy)-propionate (9.2 g, 30 mmole) in 150 ml benzene was added tetrabutylammonium bromide (1.62 g, 5 mmole) and 100 ml water. The mixture was cooled to about 5° C. and potassium permanganate (14.82 g, 90 mmole) was added in portions. The mixture was stirred 2 hours at room temperature, diluted with water and decolorized by the addition of sodium bisulfite. The mixture was acidified with 2M hydrogen chloride and extracted 3 times with ethyl acetate. The combined organic phases were washed with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product isolated by silica gel column chromatography with hexane/ethyl acetate. Yield: 5.4 g=55%. The compound can be activated and esterified to a drug or further modified as described below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-bcc8e27aeab242b28597087af1c81f63
Source noteuspto-grants-2006_07