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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492341Generated: October 30, 2026

Acetic Acid → HCID 14800099, compound

https://huagongshe.com/reaction/1492341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 11254375HCID 11254375—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14800099HCID 14800099—

Reaction Steps

4-Chlorobenzaldehyde (0.464 g) , 5α-androstan-17β-amine (4.40 g) , glacial acetic acid (0.99 g), sodium cyanoborohydride (0.21 g) and tetrahydrofuran (5 ml) were added to methanol (11 ml). The resulting mixture was warmed to dissolve the solid in solution and allowed to stir overnight at room temperature. Excess solvent was removed under reduced pressure. Water was added and made basic (pH 9) with 50% aqueous NaOH. The mixture was extracted with ether and the organic layer became cloudy. Celite was used to filter the organic layer. The aqueous layer was washed with ether and the combined organic layers were dried (NaSO4), filtered and concentrated. The crude solid was mixed with 10 g of flash silica gel and dissolved in ethyl acetate. The solvent was removed and the silica was poured on top of the chromatographic column. The compound was eluted with 50% ethyl acetate-hexane. The title compound was obtained as a solid which was recrystallized from acetone (0.364 g) mp 101°-102° C. (PLA2, diabetes)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05373095
Source datasetuspto-grants-1994_12
ORD IDord-7d721c870ffd44d3aa4914595ad38b97
Source noteuspto-grants-1994_12