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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508356Generated: October 31, 2026

Sodium Chloride → 1,4-Dioxa-8-azaspiro(4.5)decane

https://huagongshe.com/reaction/1508356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dioxa-8-azaspiro[4.5]decane--hydrogen chloride (1/1)HCID 16218795—
SolventWaterHCID 962—
Product1,4-Dioxa-8-azaspiro(4.5)decaneHCID 6743593.8%

Reaction Steps

To a 30 L reactor equipped with a mechanic stirrer, an addition funnel and a septum was charged sodium hydroxide (NaOH, 1.4 kg, 35 mol, 2.0 equiv) and water (7 L) and the resulting solution was treated with 1,4-dioxa-8-azaspiro[4.5]decane hydrochloride (3.13 kg, 17.43 mol) at ambient temperature. The resulting mixture was then stirred at ambient temperature for 30 minutes before being saturated with solid sodium chloride (1.3 kg) and extracted with 2-methyl-tetrahydrofuran (3×7 L). The combined organic phase was dried with anhydrous sodium sulfate (Na2SO4, 1.3 kg) and concentrated under reduced pressure (70 mmHg) at 50° C. after removal of the drying reagent, sodium sulfate (Na2SO4), by filtration. The yellow oil thus obtained was distilled under reduced pressure (80 mmHg, by 115 to 120° C.) to afford 1,4-dioxa-8-azaspiro[4.5]decane (2.34 kg, 2.496 kg theoretical, 93.8%) as a clear oil, which was used directly in the subsequent coupling reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221845B2
Source datasetuspto-grants-2015_12
ORD IDord-0d124a7bb7c94b7ca2d0ff33af45ef20
Source noteuspto-grants-2015_12