Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249125Generated: October 26, 2026

Methylhydrazine → Farnesylamine

https://huagongshe.com/reaction/249125

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 lM 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 numberUS05212164
Source datasetuspto-grants-1993_05
ORD IDord-74dae765f8204675be713a5ad2f4aedb
Source noteuspto-grants-1993_05