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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748884Generated: October 26, 2026

Ethyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylate → ethyl 1-{N-[(methyloxy)carbonyl]-L-valyl}-8-oxa-1-azaspiro[4.5]decane-2-carboxylate

https://huagongshe.com/reaction/1748884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylateHCID 58313084—
ReactantCarbamic acid, N-[(1S)-1-(chlorocarbonyl)-2-methylpropyl]-, methyl esterHCID 86654825—
CatalystCID 101611454HCID 178509332—
SolventDichloromethaneHCID 6344—
Productethyl 1-{N-[(methyloxy)carbonyl]-L-valyl}-8-oxa-1-azaspiro[4.5]decane-2-carboxylateHCID 5831306920%

Reaction Steps

To a solution of ethyl 8-oxa-1-azaspiro[4.5]decane-2-carboxylate (166) (125 mg, 0.59 mmol) in anhydrous dichloromethane (2 mL) was added silver cyanide (98 mg, 0.73 mmol) followed by N-[(methyloxy)carbonyl]-L-valyl chloride (142 mg, 0.73 mmol) as a solution in anhydrous dichloromethane (3.5 mL) and the solution stirred at room temperature for 18 h under nitrogen. The reaction is filtered and treated with methanol and stirred for 5 minutes. The reaction is concentrated in vacuo and the residue purified by silica gel chromatography eluting with 30-100% hexanes/EtOAc to afford the title compound as a white solid (43 mg, 20% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150587B2
Source datasetuspto-grants-2015_10
ORD IDord-a1f8079401ca44db9163679a0404ec5a
Source noteuspto-grants-2015_10