HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684689Generated: November 1, 2026
Triethylamine → 8-t-Butyl-1-oxaspiro(4,5)decane-3-one oxime
https://huagongshe.com/reaction/1684689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 8-t-Butyl-1-oxaspiro(4,5)decane-3-one | HCID 15182818 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-t-Butyl-1-oxaspiro(4,5)decane-3-one oxime | HCID 86750119 | 99.3% |
Reaction Steps
To a solution of hydroxylamine hydrochloride (6.9 g, 0.1 mol) and triethylamine (10.0 g, 0.1 mol) in 10 ml of water was added 8-t-butyl-1-oxaspiro(4,5)decane-3-one (16.0 g, 0.076 mol) in 30 ml tetrahydrofuran. The mixture was stirred at room temperature for 3 hours and at 60° C. for 1 hour. The solvent was then evaporated in vacuo and the residue was partitioned between toluene and brine (100 ml each). The organic layer was washed with brine, dried (MgSO4) and evaporated in vacuo to yield a colourless oil (17.0 g) which crystallised on standing. Recrystallisation from light petroleum gave two fractions of colourless crystals (6.6 g and 5.3 g) mp.: 118-120 and 105°-108° C. 1H-NMR indicated mixtures of geometric isomers (E/Z) in ratios of 1:1 and 2:1 respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05641883 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-092832722e8f4400b3ec1212a330ac78 |
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| Source note | uspto-grants-1997_06 |
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