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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607443Generated: October 31, 2026

Ethanol → HCID 11779533, compound

https://huagongshe.com/reaction/1607443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium BicarbonateHCID 14013—
ReactantHCID 14579591HCID 14579591—
ProductHCID 11779533HCID 11779533—

Reaction Conditions

Temperature125 °C

Reaction Steps

2,7-Difluoro-4-methyl-9-fluorenone (1.3 g, 0.0056 mol), potassium cyanide (3 eq, 0.017 mol, 1.1 g), ammonium bicarbonate (3 eq, 0.017 mol, 1.3 g), and 50 mL of ethanol were placed in a sealed bomb and heated at 125° C. for 20 h. The bomb was cooled to room temperature and the contents were filtered through Celite washing with water and ethyl acetate. The filtratewas concentrated in vacuo and the residue was dissolved in 40 mL of 1N aqueous sodium hydroxide and washed with ethyl acetate (2×30 mL). The aqueous solution was acidified with concentrated hydrochloric acid and the product extracted into ethyl acetate. The organic solution was then dried and concentrated providing 1.1 g of a crude white solid which was recrystallized from ethanol to give 340 mg of 2,7-difluoro-4-methylspiro(9H-fluorene-9,4'-imidazolidine)-2',5'-dione: mp>320° C.; 1H NMR (DMSO-d6, 60 mHz) δ 8.5 (s, 1H), 7.8 (m, 1H), 7.2 (m, 4H), 2.7 (s, 3H); IR (KBr) 3300, 1710, 1380, 770 cm-1 ; MS m/z 300 (M+), 229 (base peak). Analysis Calculated for C16H10F2N2O2.1/2H2O: C, 62.14; H, 3.58; N, 9.06. Found: C, 62.21; H, 3.58; N, 8.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04864028
Source datasetuspto-grants-1989_09
ORD IDord-8891f026d3d04de7b90674995d691074
Source noteuspto-grants-1989_09