HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070076Generated: October 25, 2026
Acetic Acid → ethyl (8E)-8-[(4-hydroxyphenyl)methoxyimino]-8-phenyloctanoate
https://huagongshe.com/reaction/1070076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ethyl 8-oxo-8-phenyloctanoate | HCID 10934282 | — |
| Reactant | 4-(Tert-butyldimethylsilyloxy)benzyloxyamine | HCID 11821117 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | ethyl (8E)-8-[(4-hydroxyphenyl)methoxyimino]-8-phenyloctanoate | HCID 22344573 | 77% |
Reaction Steps
A mixture of 4-(tert-butyldimethylsilyloxy)benzyloxyamine (3.10 g), ethyl 8-oxo-8-phenyloctanoate (6.32 g), acetic acid (2.07 ml), sodium acetate (1.98 g) and ethanol (80 ml) was heated under reflux for 20 hours. The reaction mixture was cooled to room temperature, water was added and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in tetrahydrofuran (60 ml), tetrabutylammonium fluoride trihydrate (3.98 g) was added and stirred at room temperature for 1 hour. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain ethyl E-8-(4-hydroxybenzyloxyimino)-8-phenyloctanoate (3.55 g, yield 77%) as a colorless oil from an ethyl acetate-hexane (2:7, v/v)-eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251926B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-67085f1dc1d04d699cf8a76cf13a89ec |
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| Source note | uspto-grants-2001_06 |
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