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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889697Generated: October 29, 2026

4-Phenylbutanal → HCID 66616601, compound

https://huagongshe.com/reaction/1889697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylbutanalHCID 29030—
ReactantHCID 3739483HCID 3739483—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 66616601HCID 66616601622.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of (3-(4-fluorophenoxy)phenyl)methanamine (200 mg, 0.092 mmol, 1.0 eq) in methanol was added 4-phenylbutanal (136 mg, 0.92 mmol, 1.0 eq). The mixture was refluxed for 2 h, then cooled to 0° C., before adding NaBH4 (105 mg, 2.76 mmol, 3.0 eq) portion wise. The mixture was stirred for 15 minutes before being quenched with 10% aq. NaHCO3 solution. The volatiles were evaporated under reduced pressure and the aqueous solution obtained was extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to obtain the desired compound (200 mg, 62%); 1H NMR (400 MHz, CD3OD) δ 7.33-6.86 (m, 13H), 3.72-3.50 (s, 2H), 2.63-2.50 (m, 4H), 1.65-1.54 (m, 4H). MS (ESI): 350.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-be5a3eee4cbb468e955afe61549cd3bd
Source noteuspto-grants-2013_08