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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486562Generated: October 30, 2026

Fumaric Acid → HCID 19095351, compound

https://huagongshe.com/reaction/486562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19095348HCID 19095348—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 19095351HCID 1909535192%

Reaction Steps

6-(3,4-Dichlorophenyl)-3,4-dihydro-1-methylpyrrolo[1,2-a]pyrazine (1.8 g) was dissolved in a mixture of 100 ml of methanol and 10 ml of water under argon. The solution was treated portionwise with 0.7 g of sodium borohydride while stirring and stirred at room temperature overnight. Thereafter, the methanol was removed in a vacuum, the residue was taken up in 150 ml of methylene chloride and washed with 65 ml of 10% ammonia solution. The phases were separated and the aqueous phase was extracted twice with 70 ml of methylene chloride each time. The organic phases were combined, dried with MgSO4 and freed from solvent. The crude product, 1.8 g of brown oil, 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 were obtained 2.0 g (92%) of 6-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-methylpyrrolo[1,2-a]pyrazine fumarate (2:1); m.pt.: 224°-226° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292732
Source datasetuspto-grants-1994_03
ORD IDord-3e34368cbbf64308977930de17b1d44e
Source noteuspto-grants-1994_03