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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761659Generated: November 1, 2026

Sodium Hydroxide → HCID 14300213, compound

https://huagongshe.com/reaction/1761659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14300211HCID 14300211—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 14300213HCID 1430021347.9%

Reaction Steps

A solution of 8.2 g of tert.butyl 1-[5-(ethoxycarbonyl)-5-hexenoyl]-hexahydro-3-(S)-pyridazinecarboxylate in 25 ml of ethanol was treated with 23.7 ml of 1N aqueous sodium hydroxide solution for 16 hours. The solution was diluted with 80 ml of water and the volume was then reduced to 80 ml by evaporation. The solution was washed with diethyl ether and the pH of the aqueous solution was adjusted to 3 using 2N aqueous hydrochloric acid. The solution was then extracted with dichloromethane. The organic solution was evaporated and the residue was chromatographed on silica gel using dichloromethane/methanol (9:1) for the elution, whereby there were obtained 3.62 g of tert.butyl 1-[5-(carboxy)-5-hexenoyl]-hexahydro-3(S)-pyridazinecarboxylate in the form of a white solid of melting point 86°-88° C., from n-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826980
Source datasetuspto-grants-1989_05
ORD IDord-1fde4082c5c74a05b336add4cf278b33
Source noteuspto-grants-1989_05