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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224277Generated: October 31, 2026

Hydrochloric Acid → HCID 12891348, compound

https://huagongshe.com/reaction/224277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydrideHCID 166653—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
ReactantHCID 23332346HCID 23332346—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 12891348HCID 12891348—

Reaction Steps

To a stirred solution of 30 ml of sodium bis(2-methoxyethoxy)aluminum hydride (70% benzene solution) is added dropwise a solution of 5.5 g of N-methyl-1-phenyl-1,2-cyclopropanedicarboxamide (U.S. Pat. No. 3,166,571-Ex. 1) in 400 ml of benzene over a one hour period at room temperature under nitrogen. The mixture is heated at reflux under nitrogen for 90 minutes. The excess hydride reagent is decomposed by the cautious addition of 25 ml of 10 N sodium hydroxide and then diluted to 200 ml with water. The benzene phase is separated and the aqueous phase is extracted with chloroform. The combined organic phases are dried over magnesium sulfate and concentrated under reduced pressure giving a liquid. The liquid is dissolved in ethanol and acidified with 15 ml of 2.3 N ethanolic hydrogen chloride. The addition of ether causes the formation of a solid which is recrystallized from isopropyl alcohol-hexane giving white crystals, m.p. 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04231935
Source datasetuspto-grants-1980_11
ORD IDord-7b40966cc8e44493966858f510ab0285
Source noteuspto-grants-1980_11