ChemicalBook--->CAS DataBase List--->180160-97-8

180160-97-8

180160-97-8 Structure

180160-97-8 Structure
IdentificationBack Directory
[Name]

spiro[isochroman-1,4'-piperidine]
[CAS]

180160-97-8
[Synonyms]

spiro[isochroman-1,4'-piperidine]
3,4-dihydrospiro[2-benzopyran-1,4'
3,4-Dihydrospiro[isochromene-1,4'-piperidine]
3,4-dihydrospiro[2-benzopyran-1,4'-piperidine]
Spiro[1H-2-benzopyran-1,4'-piperidine], 3,4-dihydro-
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C13H17NO
[MDL Number]

MFCD16876099
[MOL File]

180160-97-8.mol
[Molecular Weight]

203.28
Chemical PropertiesBack Directory
[Boiling point ]

341.3±42.0 °C(Predicted)
[density ]

1.12
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

10.21±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

spiro[isochroman-1,4'-piperidine](180160-97-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

tert-butyl spiro[isochroman-1,4'-piperidine]-1'-carboxylate

909034-76-0

spiro[isochroman-1,4'-piperidine]

180160-97-8

The general procedure for the synthesis of spiro[isobenzodihydropyran-1,4'-piperidine]-1'-carboxylic acid tert-butyl ester from spiro[isobenzodihydropyran-1,4'-piperidine] is as follows: Step 1: Deprotection reaction Trifluoroacetic acid (15 mL) was added to a solution of tert-butyl spiro[isobenzodihydropyran-1,4'-piperidine]-1'-carboxylate (3.3 g, 10.87 mmol) in dichloromethane (15 mL), and the reaction was stirred for 2 h at room temperature. Step 2: Post-treatment The reaction mixture was concentrated under reduced pressure and the residue was redissolved in dichloromethane (15 mL). Alkalization was carried out by adjusting the pH to 8 with aqueous sodium carbonate. The organic and aqueous phases were separated and the organic phase was washed sequentially with water, sodium bicarbonate solution and saturated saline. The organic phase was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. Step 3: Purification The obtained residue was ground with ether to obtain white solid spiro[isobenzodihydropyran-1,4'-piperidine] (1.35 g, 64% yield). Characterization data: 1H NMR (DMSO-d6, 400 MHz) δ: 1.88 (m, 2H), 2.09 (m, 2H), 2.77 (t, 2H), 3.02 (m, 2H), 3.15 (m, 2H), 3.90 (t, 2H), 7.10-7.28 (m, 4H). LRMS: m/z APCI+ 204 [MH]+.

[References]

[1] Patent: WO2006/92731, 2006, A1. Location in patent: Page/Page column 42
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