Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 13732928 | HCID 13732928 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13732944 | HCID 13732944 | 63% |
Reaction Steps
A mixture of 10.81 g of spiro[benzofuran-2(3H),1'-cycloheptane]-3-one, 100 ml of absolute ethanol, 34.75 g of hydroxylamine hydrochloride and 100 ml of pyridine was heated at reflux overnight under nitrogen and thereafter cooled to room temperature. The mixture was poured into 500 ml of 2N aqueous hydrochloric acid and extracted with hexane (2×200 ml). The combined hexane extracts were washed with 2N hydrochloric acid (100 ml), distilled water (100 ml) and saturated sodium chloride solution (100 ml). After the last wash, the oxime began to crystallize out of the hexane extracts; dichloromethane was added to redissolve any crystallized solid and the solution was dried overnight over anhydrous sodium sulfate. Filtration and concentration in vacuo afforded a gum which was triturated to solid with hexane. This material was filtered off and recrystallized from 60 ml of boiling hexane to afford 7.28 g of needles, m.p. 98.5°-103.5° C. Recrystallization twice more from 60 ml portions of hexane afforded 5.01 g of pure major (Z) isomer as needles, m.p. 104°-106.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04623657 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-0575c5276df2453184e6a72c741b5248 |
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| Source note | uspto-grants-1986_11 |
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