Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580043Generated: October 31, 2026

Dimethylformamide → 8-(2-Quinolinyl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/580043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChloroquinolineHCID 11928—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product8-(2-Quinolinyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 1415639422%

Reaction Steps

A mixture of 10 g (0.0613) of 2-chloroquinoline, 27 g (0.1886 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, 13 g (0.0941) of K2CO3, and 75 ml of dimethylformamide is stirred at 100°-110° C. for 4 days. The reaction mixture is allowed to cool to ambient temperature, diluted with water and extracted with ethyl acetate. The combined organic extracts are washed copiously with water, then brine, dried over Na2SO4, and concentrated in vacuo to give a waxy solid. Trituration with ether furnishes 3.6 g (22%) of title compound: IR (KBr) 1620, 1610 and 1510 cm-1 ; NMR (CDCl3) δ7.92 (d, 1H), 7.78-7.50 (m, 3H), 7.30-7.22 (m, 1H), 7.04 (d, 1H), 4.02 (s, 4H), 3.94-3.86 (m, 4H), and 1.88-1.76 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751305
Source datasetuspto-grants-1988_06
ORD IDord-210dd6efd9a54096b1be43afbd9069c0
Source noteuspto-grants-1988_06