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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543502Generated: October 30, 2026

N-Carbethoxyphthalimide → HCID 20461678, compound

https://huagongshe.com/reaction/543502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-CarbethoxyphthalimideHCID 31187—
ReactantHCID 13116879HCID 13116879—
SolventBenzeneHCID 241—
ProductHCID 20461678HCID 20461678—

Reaction Steps

A mixture of crude 1.1-difluoro-2-amino-4-methyl-4-pentene (20 g, evaluated 110 mmoles) prepared as in Step A above, N-carbethoxyphthalimide (24 g, 110 mmoles) in benzene (300 mL) is kept overnight at room temperature. The solution is concentrated under vacuum, the oily residue is dissolved in methylene chloride (400 mL) and treated with 8 g of triethylamine during one night at room temperature. The solution is extracted with water, twice with 1 N hydrochloric acid and twice with water again. Evaporation of the organic layer affords an oily residue which is crystallized from petroleum ether at -5° C. (19.2 g, yield based on methallyl chloride: 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446151
Source datasetuspto-grants-1984_05
ORD IDord-1c8f306f1c484227b29860c8f0086ea2
Source noteuspto-grants-1984_05