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301226-27-7

301226-27-7 Structure

301226-27-7 Structure
IdentificationBack Directory
[Name]

tert-butyl 2-oxo-1-oxa-8-azaspiro[4.5]decane-8-carboxylate
[CAS]

301226-27-7
[Synonyms]

8-Boc-2-oxo-1-oxa-8-azaspiro[4.5]decane
8-Boc-2-oxo-1-oxa-8-azaspiro[4.5]decane - X11712
1,1-diMethylethyl 1-oxa-2-oxo-8-azaspiro[4.5]decane-8-carboxylate
2-Oxo-1-oxa-8-azaspiro[4.5]decane-8-carboxylic acid 1,1-dimethylethyl ester
1-Oxa-8-azaspiro[4.5]decane-8-carboxylic acid, 2-oxo-, 1,1-dimethylethyl ester
[Molecular Formula]

C13H21NO4
[MDL Number]

MFCD11100196
[MOL File]

301226-27-7.mol
[Molecular Weight]

255.31
Chemical PropertiesBack Directory
[Boiling point ]

399.6±35.0 °C(Predicted)
[density ]

1.16±0.1 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

-0.84±0.20(Predicted)
[Appearance]

White to off-white Solid
[InChI]

1S/C13H21NO4/c1-12(2,3)18-11(16)14-8-6-13(7-9-14)5-4-10(15)17-13/h4-9H2,1-3H3
[InChIKey]

DXCDANAWBPYOAA-UHFFFAOYSA-N
[SMILES]

O=C(OC(C)(C)C)N(CC1)CCC12OC(CC2)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 2-oxo-1-oxa-8-azaspiro[4.5]decane-8-carboxylate(301226-27-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Piperidinepropanoic acid, 1-[(1,1-diMethylethoxy)carbonyl]-4-hydroxy-, ethyl ester

374794-91-9

tert-butyl 2-oxo-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

301226-27-7

4-(3-Ethoxy-3-oxopropan-1-yl)-4-hydroxy-1-piperidinecarboxylic acid 1,1-dimethylethyl ester (27.63 g, 0.092 mol) was used as raw material and dissolved in toluene (250 mL). To this solution was added p-toluenesulfonic acid (1.75 g, 9.2 mmol) and the mixture was heated to reflux for 3 hours. After the reaction was complete, the mixture was cooled and the solvent was removed by evaporation under reduced pressure. Water (400 mL) and ethyl acetate (400 mL) were added to the residue to separate the organic and aqueous layers. The aqueous layer was further extracted with ethyl acetate (200 mL). All organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to afford 1-oxo-8-N-BOC-azaspiro[4.5]decan-2-one (20.86 g, 88% yield). The mass spectrum (electrospray positive ion mode) showed m/z 256 ([M+1]+).

[References]

[1] Patent: US2003/236250, 2003, A1. Location in patent: Page 29
[2] Patent: WO2004/78750, 2004, A1. Location in patent: Page 79-80
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 13, p. 1759 - 1762
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