Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482150Generated: November 1, 2026

Sodium cyanoborohydride → HCID 19065570, compound

https://huagongshe.com/reaction/482150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 73516783HCID 73516783—
SolventAcetic AcidHCID 176—
ProductHCID 19065570HCID 1906557057.4%

Reaction Steps

To a stirred solution of 3-[3-(4-fluorophenoxy)phenyl]-2-cyclopentenone oxime (1.85 g; 6.54 mM) in acetic acid (10 ml) was added sodium cyanoborohydride (0.62 g; 9.81 mM) portionwise at room temperature. After stirring for 2 hrs, additional sodium cyanoborohydride (0.25 g; 4 mM) and acetic acid (5 ml) was added. The mixture was stirred overnight. Acetic acid was removed in vacuo, and to the residue was added saturated aqueous NaHCO3 (50 ml). The whole was extracted with ethyl acetate (50 ml×1, 30 ml×1), and the combined organic layers were washed with water (50 ml), brine (50 ml), dried over MgSO4, and concentrated in vacuo. The residual oil was purified by flash column (SiO2) eluting with CH2Cl2 -ethanol (30:1) to give 1.07 g of the subtitle compound [F] as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792882
Source datasetuspto-grants-1998_08
ORD IDord-4924d31f898f4f84bfe17a1e2fcc338d
Source noteuspto-grants-1998_08