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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757402Generated: October 31, 2026

Water → HCID 19387925, compound

https://huagongshe.com/reaction/1757402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetonitrileHCID 7856—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantHCID 178418922HCID 178418922—
SolventDimethylformamideHCID 6228—
ProductHCID 19387925HCID 1938792550%

Reaction Steps

To a mixture of 16.8 g (0.1 mol) N-hydroxyphthalimide and 12.7 g (0.11 mol)tert-BuOK in 150 mL DMF under stirring was added cyanomethyl chloride (7.8 g, 0.1 mol). Discoloration of the reaction mixture occurred in 10 min. After 24 h of stirring at room temperature the mixture was poured into 750mL of cold H2O. Precipitate was filtered off and dried under vacuum in the presence of anhydrous CaSO4 to yield about 10 g (50%) of cyanomethoxyphthalimide. To a solution of 10 g (0.05 mol) cyanomethoxyphthalimide in 50 mL THF was added dropwise at room temperature during 2 h a solution of 2.5 mL (0.05 mol) hydrazine-hydrate (100%) in 10 mL MeOH. After additional stirring for 2 h the mixture was acidified under ice-cooling with 25 mL of 2M solution (0.05 mol) HCl and the resulting mixture was stirred at this temperature for 30 min. The insoluble material was filtered off, filtrate adjusted to pH 7 with 2M NaOH. The product was then extracted 4 times with EtOAc, the combined organics were washed with brine, and dried over anhydrous Na2SO4. The solution was concentrated in vacuo, the residue was dissolved in ether and treated with an excess of dry hydrogen chloride. The title compound, a precipitate, was filtered off and dried under vacuumin the presence of anhydrous CaSO4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446048
Source datasetuspto-grants-1995_08
ORD IDord-4f7c2015e0a449d89a927db8aa3b99aa
Source noteuspto-grants-1995_08