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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605649Generated: November 1, 2026

Acetone → HCID 21547089, compound

https://huagongshe.com/reaction/1605649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodiumHCID 5360545—
ReactantHCID 21547110HCID 21547110—
ReactantHCID 178418361HCID 178418361—
CatalystNickel acetate tetrahydrateHCID 62601—
Catalystnickel boride (NiB)HCID 82791—
SolventEthanolHCID 702—
ProductHCID 21547089HCID 2154708962.1%

Reaction Steps

15 Gm (0.06 mol) of nickel(II)acetate tetrahydrate, dissolved in 600 ml of 95% ethanol, were reduced to black, colloidal nickel boride (P-2-catalyst) in a hydrogenation vessel with 60 ml of 1 M sodium borohyride solution in an atmosphere of hydrogen. In order to remove any unreacted borohydride which may be present, 14 gm (0.24 mol) of acetone were first added and the mixture was shaken for one hour at room temperature. Thereafter, 30.0 gm (0.123 mol) of (E)-4-(2'-fluoro-4-biphenylyl)-3-buten-2-one were added, and the mixture was hydrogenated at room temperature and 5 atmospheres until the absorption of hydrogen terminated. Subsequently, the catalyst was filtered off, the filtrate was evaporated in vacuo, and the residue was shaken with a mixture of water and ethyl acetate. The organic phase was dried over sodium sulfate and then evaporated, and the residue was distilled in a high vacuum, yielding 18.5 gm (62% of theory) of 4-(2'-fluoro-4-biphenylyl)-2-butanone in the form of a colorless, viscous oil having a boiling point of 153°-155°C at 0.4 mm Hg which solidified after prolonged standing and then had a melting point of 30°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950427
Source datasetuspto-grants-1976_04
ORD IDord-37a8dffdab874fcd8f5ac5f562c3a7ea
Source noteuspto-grants-1976_04