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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327902Generated: October 26, 2026

Methylhydrazine → Farnesylamine

https://huagongshe.com/reaction/327902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantSodium HydroxideHCID 14798—
Reactant2-(3,7,11-Trimethyl-2,6,10-dodecatrienyl)-1H-isoindole-1,3(2H)-dioneHCID 54205188—
SolventEthanolHCID 702—
ProductFarnesylamineHCID 308063089%

Reaction Steps

A solution 2.50 g (7.1 mmol) of Part (1) compound in 15 ml of absolute ethanol at room temperature under argon was treated with 1.9 ml (35.57 mmol, 5.0 eq.) of methyl hydrazine and stirred for 2 hours at room temperature and 4 hours at reflux. After cooling and the addition of 7.1 ml (7.1 mmol, 1.0 eq.) of 1M NaOH, the ethanol was removed under reduced pressure. The residue was extracted with 350 ml of ethyl ether and the ether layer washed with 100 ml of 1M NaOH, 50 ml of H2O and 50 ml of brine, dried (MgSO4) and evaporated to obtain 1.45 g of crude product. Purification by bulb-to-bulb distillation at 120° C./0.005 mm provided 1.405 g (89%) of title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273969
Source datasetuspto-grants-1993_12
ORD IDord-5b1efbb6a5584d7b880fc32340c01302
Source noteuspto-grants-1993_12