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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188000Generated: October 29, 2026

Hydrazine → HCID 21936680, compound

https://huagongshe.com/reaction/2188000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 21936658HCID 21936658—
SolventEthanolHCID 702—
ProductHCID 21936680HCID 2193668063.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of the above 2-(1,4-dioxa-8-aza-spiro[4.5]dec-7-ylmethyl)isoindole-1,3-dione (3.85 mmol) in absolute ethanol (25 ml) was added hydrazine (0.36 ml, 11.55 mmol). The reaction was stirred at 80° C. (oil bath) for 6 hours, then cooled to ambient temperature and stirred for an additional 12 hours. The thick precipitate was filtered off and washed with ethanol. The filtrate was concentrated in vacuo and reconstituted in dichloromethane (20 ml), forming a small amount of a second precipitate, which was filtered off. The filtrate was evaporated in vacuo and the resulting oil was dissolved in water (10 ml) and basified with 1 N sodium hydroxide until pH=10. The aqueous layer was extracted with 20% isopropyl alcohol/chloroform (12×40 ml). The combined organic extracts were dried (K2CO3), filtered and the solvent evaporated in vacuo affording 0.42 g (63%) of (1,4-dioxa-8-aza-spiro[4.5]dec-7-yl)methylamine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410556B1
Source datasetuspto-grants-2002_06
ORD IDord-306e7d4168d2449baefd5d1ed5f5527e
Source noteuspto-grants-2002_06