Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382850Generated: October 25, 2026

Acetonitrile → Ethyl 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzoate

https://huagongshe.com/reaction/1382850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
ReactantBenzoic acid, 4-fluoro-, ethyl esterHCID 67976—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthyl 4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)benzoateHCID 1271743930.5%

Reaction Steps

A mixture of 50 g (0.349 mol) of ethyl p-fluorobenzoate, 185 g (1.29 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, 73 g (0.5282 mol) of K2CO3, and 400 ml of acetonitrile is stirred at 90°-100° C. for three days. The reaction mixture is allowed to cool to ambient temperature, diluted with water, and extracted with methylene chloride. The combined organic extracts are washed with brine, dried over Na2SO4, and concentrated in vacuo to give a pasty solid. Trituration with ether furnishes 31 g (23%) of title compound: IR (KBr) 1695 and 1610 cm-1 ; NMR (CDCl3) δ7.98 (d, 2H), 6.96 (m, 2H), 4.36 (q, 2H), 4.02 (s, 4H), 3.58-3.48 (m, 4H), 1.92-1.80 (m, 4H), and 1.38 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808612
Source datasetuspto-grants-1989_02
ORD IDord-6b8a15b6b42e438e8dcfeb14585ca7ed
Source noteuspto-grants-1989_02