HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482150Generated: November 1, 2026
Sodium cyanoborohydride → HCID 19065570, compound
https://huagongshe.com/reaction/482150
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 73516783 | HCID 73516783 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19065570 | HCID 19065570 | 57.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792882 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-4924d31f898f4f84bfe17a1e2fcc338d |
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| Source note | uspto-grants-1998_08 |
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