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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486565Generated: October 30, 2026

Fumaric Acid → HCID 19095307, compound

https://huagongshe.com/reaction/486565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19095284HCID 19095284—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 19095307HCID 1909530724%

Reaction Steps

5,6,10,11-Tetrahydro-8-methylbenzo[g]pyrazino[1,2-a]indole (0.6 g) was dissolved in a mixture of 25 ml of ethanol and 2.5 ml of water under argon. The solution was treated portionwise with 0.3 g of sodium borohydride while stirring and stirred at room temperature overnight. Thereafter, the solvent was removed in a vacuum, the residue was taken up in 50 ml of methylene chloride and washed with 50 ml of 10% ammonia solution. The phases were separated and the aqueous phase was extracted twice with 20 ml of methylene chloride each time. The organic phases were combined, dried with MgSO4 and freed from solvent. The crude product, 0.5 g of brown solid, was dissolved in a 20-fold amount of ethanol and treated with 1.1 equivalents of a saturated solution of fumaric acid in ethanol. There was obtained 0.2 g (24%) of 5,6,8,9,10,11-hexahydro-8-methylbenzo[g]pyrazino[1,2-a]indole fumarate (1:1); m.pt.: 181°-184° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292732
Source datasetuspto-grants-1994_03
ORD IDord-dbeb29a497964cbfbe2a42e9b687be54
Source noteuspto-grants-1994_03