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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279175Generated: October 31, 2026

Hydrazine hydrate (1:1) → 3,6,9,12,15-Pentaoxaheptadecane-1,17-diamine

https://huagongshe.com/reaction/1279175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 18427234HCID 18427234—
SolventEthanolHCID 702—
Product3,6,9,12,15-Pentaoxaheptadecane-1,17-diamineHCID 1561019197.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

The synthesis generally followed the method of Kern et al., Makrol. Chem., 180, 2539 (1979). A solution containing 60 g of 1,17-diphthalimido-3,6,9,12,15-pentaoxaheptadecane (0.118 mol), 14.8 g of hydrazine hydrate (0.296 mol), and 500 mL of ethanol is heated with mechanical stirring in a 100° C. oil bath for three hrs. The mixture is cooled and filtered. A resultant filter cake is washed four times with 300 mL portions of ethanol. The combined filtrates are concentrated to yield 32.35 g of a yellow opaque glassy oil by evaporative distillation at 150-200° C. (0.01 mm of vacuum). The result is 22.82 g of a light yellow oil (69% yield). b.p. 175-177° C. (0.07 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448047B2
Source datasetuspto-grants-2002_09
ORD IDord-5a7066d196a2471487373230fff0da29
Source noteuspto-grants-2002_09