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

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tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate Basic information
Uses
Product Name:tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate
Synonyms:tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate;1-Boc-2-oxo-8-azaspiro-[4.5]decane-8-carboxylic acid;2-OXO-8-AZA-SPIRO[4.5]DECANE-8-CARBOXYLIC ACID TERT-BUTYL ESTER;8-Azaspiro[4.5]decane-8-carboxylic acid, 2-oxo-, 1,1-dimethylethyl ester;8-Boc-8-azaspiro[4.5]decan-2-one;1-Boc-2-oxo-8-azaspiro[4.5]decane-8-carboxylic acid - [X13487];1,1-Dimethylethyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate;tert-butyl 3-oxo-8-azaspiro[4.5]decane-8-carboxylate
CAS:1250994-14-9
MF:C14H23NO3
MW:253.34
EINECS:
Product Categories:1
Mol File:1250994-14-9.mol
tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate Structure
tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate Chemical Properties
Boiling point 365.0±35.0 °C(Predicted)
density 1.10±0.1 g/cm3(Predicted)
storage temp. Storage temp. 2-8°C
pka-0.77±0.20(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C14H23NO3/c1-13(2,3)18-12(17)15-8-6-14(7-9-15)5-4-11(16)10-14/h4-10H2,1-3H3
InChIKeyZXXJXEXKMUZKPG-UHFFFAOYSA-N
SMILESC1C2(CCN(C(OC(C)(C)C)=O)CC2)CCC1=O
Safety Information
MSDS Information
tert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate Usage And Synthesis
Usestert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate is a useful research chemical.
Synthesis
N-Methyl-N-nitrosotoluene-4-sulphonamide

80-11-5

tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate

203661-69-2

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

1250994-14-9

A 10% to 40% aqueous solution of potassium hydroxide (20 mL) was added to a solvent mixture of tetrahydrofuran and methanol containing tert-butyl-2-oxo-7-azaspiro[3.5]nonane-7-carboxylic acid (8.2 g). The solvent ratio was 10:1. In another vessel, N-methyl-N-nitroso-p-toluenesulfonamide (19.6 g) was dissolved in 300 mL of water and added slowly and dropwise at 0 °C to the above reaction solution. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the system was cooled to room temperature and the reaction was quenched by the addition of acetic acid. Subsequently, the reaction mixture was rotary evaporated to dryness and the residue was dissolved in ethyl acetate (100 mL) and washed sequentially with water (100 mL) and saturated brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by column chromatography afforded ethyl tert-butyl-2-oxo-8-azaspiro[4.5]decane-8-carboxylate (6.6 g, yield: 72%).

References[1] Patent: CN105272914, 2016, A. Location in patent: Paragraph 0010; 0014
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