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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871846Generated: October 31, 2026

Hydrochloric Acid → HCID 86673132, compound

https://huagongshe.com/reaction/871846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantCyanoacetamideHCID 7898—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178521536HCID 178521536—
SolventWaterHCID 962—
ProductHCID 86673132HCID 866731329%

Reaction Conditions

Temperature3.5 °C

Reaction Steps

To a solution, cooled to 2-5°C. on an ice bath, of 1.88 g (22.41 mmol) of cyanoacetamide in 20 mL of anhydrous DMF are added portionwise 1.8 g (44.82 mmol) of 60% sodium hydride. The mixture is stirred for 15 minutes at 2-5°C., and this suspension is then added rapidly to a solution of 5.2 g (21.34 mmol) of the acid fluoride prepared in step 3.2 in 20 mL of anhydrous DMF precooled to 2-5°C. The mixture is stirred overnight at room temperature and then cooled to 2-5°C. on an ice bath, and 0.90 g (22.41 mmol) of 60% sodium hydride is added portionwise. The reaction mixture is stirred for 3 hours at room temperature and then poured into a mixture of ice, 100 mL of water and 150 mL of aqueous 1N HCl. The yellow precipitate formed is isolated by filtration, rinsed with water and then dried in an oven, after which it is rinsed with pentane. 5.4 g of a mixture containing the expected cyclized product and the non-cyclized product are finally obtained in the form of an orange powder. The mixture is purified by chromatography on a column of silica, eluting with a dichloromethane/methanol gradient (99/1 to 96/4). 0.6 g of the expected product is finally obtained in the form of a pale yellow solid. Yield=9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-eafd4143468d4c4e8eb8fb9e08ceaeac
Source noteuspto-grants-2015_03