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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656248Generated: October 28, 2026

Ammonium Hydroxide → (1S)-6-Oxaspiro[2.5]octane-1-carboxamide

https://huagongshe.com/reaction/656248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 57429840HCID 57429840—
SolventEthyl AcetateHCID 8857—
Product(1S)-6-Oxaspiro[2.5]octane-1-carboxamideHCID 57429839—

Reaction Steps

18.85 g of carbonyldiimidazole are added to a solution of 17.66 g of (S)-6-oxaspiro[2.5]-octane-1-carboxylic acid (prepared in analogy to building block FFFFa from (R)-4-benzyl-3-((S)-6-oxaspiro[2.5]-octane-1-carbonyl)oxazolidin-2-one (building block FFFFb)) in 330 ml of ethyl acetate. The reaction solution is left to stand at room temperature for 6 hours and then 330 ml of 25% ammonium hydroxide solution are added. The reaction mixture is stirred at room temperature for 16 hours, the phases are separated, and the aqueous phase is extracted with ethyl acetate. The combined organic phases are washed with water until neutral, dried with sodium sulphate and evaporated. The title compound is obtained from the residue by flash chromatography (SiO2 60 F) as a yellowish oil which may crystallize if sufficiently pure. Rf=0.28 (dichloromethane-methanol-conc. ammonia 25% 200:20:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071651B2
Source datasetuspto-grants-2011_12
ORD IDord-d9eb3787e12c4fa798c94bc4e7e7846b
Source noteuspto-grants-2011_12