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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380336Generated: November 2, 2026

Acetone → HCID 10478752, compound

https://huagongshe.com/reaction/2380336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10431342HCID 10431342—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 10478752HCID 10478752—

Reaction Steps

To a solution of ethyl 6-{[4-(4-aminophenyl)-6-phenyl-2-pyridyl]oxy}hexanoate (3 g) and acetone (0.54 cc) in acetic acid (45 cc), brought to 15° C., is slowly added sodium borohydride (1.14 g) so as to maintain the temperature below 22° C. The mixture is then stirred at room temperature for 4 hours. The reaction mixture is then poured in distilled water (150 cc) and extracted with ethyl ether (2×100 cc). The combined organic phases are washed with distilled water until neutrality, dried over sodium sulphate and concentrated to dryness at 40° C. under reduced pressure. The oily residue obtained is purified by chromatography under pressure on silica gel (30-60 mm; eluent: n-hexane-ethyl acetate 9-1 as a yellow oil)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366982
Source datasetuspto-grants-1994_11
ORD IDord-9dd82c2b7e41470babbee4d481c00f42
Source noteuspto-grants-1994_11