Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232554Generated: November 3, 2026

Triethylamine → 8-t-Butyl-1-oxaspiro(4,5)decane-3-one oxime

https://huagongshe.com/reaction/232554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant8-t-Butyl-1-oxaspiro(4,5)decane-3-oneHCID 15182818—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product8-t-Butyl-1-oxaspiro(4,5)decane-3-one oximeHCID 8675011999.3%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591741
Source datasetuspto-grants-1997_01
ORD IDord-856286c2b09c4fef89daa4f589af7cc1
Source noteuspto-grants-1997_01