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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194690Generated: October 25, 2026

Acetonitrile → 8-Octyl-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/1194690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodooctaneHCID 12380—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
SolventWaterHCID 962—
Product8-Octyl-1,4-dioxa-8-azaspiro[4.5]decaneHCID 2124928090%

Reaction Steps

To a mixture of 15 g (0.105 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, 15.93 g (0.115 mol) of K2CO3, and 100 ml of acetonitrile is added dropwise 18.92 ml (0.105 mol) of iodooctane. The mixture is stirred overnight at room temperature and then at 65° C. for 2 hours. After cooling, the mixture was diluted with water and extracted with methylene chloride. The combined extracts are washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue is triturated with ether and filtered. The filtrate is concentrated in vacuo to yield 24.04 g (90%) of title compound as a clear oil: IR (neat) 2925 and 1094 cm-1 ; NMR (CDCl3) δ3.97 (s, 4H), 2.56 (br, 4H), 2.38 (m, 2H), 1.78 (m, 4H), 1.51 (br, 2H), 1.28 (s, 10H), 0.89 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816464
Source datasetuspto-grants-1989_03
ORD IDord-1304b6314bb14c6dbf27df954ac43158
Source noteuspto-grants-1989_03