spiro<benzofuran-3(2H),4'-piperidine
- Product Name
- spiro<benzofuran-3(2H),4'-piperidine
- CAS No.
- 171-77-7
- Chemical Name
- spiro<benzofuran-3(2H),4'-piperidine
- Synonyms
- spiro;2H-Spiro[benzofuran-3,4'-piperidine];spiro
- CBNumber
- CB12561087
- Molecular Formula
- C12H15NO
- Formula Weight
- 189.25
- MOL File
- 171-77-7.mol
spiro<benzofuran-3(2H),4'-piperidine Property
- Boiling point:
- 320.4±42.0 °C(Predicted)
- Density
- 1.14±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 10.60±0.20(Predicted)
Safety
- HS Code
- 2933399990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 7755CV
- Product name
- 2H-Spiro[benzofuran-3,4'-piperidine]
- Packaging
- 100mg
- Price
- $181
- Updated
- 2021/12/16
- Product number
- CHM0388246
- Product name
- 2H-SPIRO[BENZOFURAN-3,4'-PIPERIDINE]
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.88
- Updated
- 2021/12/16
- Product number
- 7755CV
- Product name
- 2H-Spiro[benzofuran-3,4'-piperidine]
- Packaging
- 1g
- Price
- $546
- Updated
- 2021/12/16
- Product number
- 4H56-1-345
- Product name
- 2H-Spiro[1-benzofuran-3,4'-piperidine]
- Purity
- 97%
- Packaging
- 250mg
- Price
- $640
- Updated
- 2021/12/16
- Product number
- 4H56-1-345
- Product name
- 2H-Spiro[1-benzofuran-3,4'-piperidine]
- Purity
- 97%
- Packaging
- 1g
- Price
- $1280
- Updated
- 2021/12/16
spiro<benzofuran-3(2H),4'-piperidine Chemical Properties,Usage,Production
Synthesis
72374-35-7
171-77-7
Preparation of Example 20: A suspension of 1-benzyl-spiro[benzofuran-3,4-piperidine] (1.0 g, 3.58 mmol) was formed with 10% palladium carbon (750 mg) in ethanol (30 mL). To this suspension was added spiro H-benzofuran-3,4'-piperidine ammonium formate (1.13 g, 17.94 mmol) in one go. The reaction mixture was heated to reflux for 1.25 hours. After completion of the reaction, the mixture was cooled, filtered through Arbocel and the filter cake was washed with additional ethanol. The filtrate was evaporated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using a gradient elution of dichloromethane: methanol: 0.88 ammonia (100:0:0 to 90:10:1) to give 2H-spiro[benzofuran-3,4'-piperidinium] as a cream-colored solid (489 mg, 72% yield). The product was confirmed by 1HNMR (CDCl3, 400MHz): δ 1.72 (m, 2H), 1.80-1.96 (m, 2H), 2.70 (m, 2H), 3.11 (m, 2H), 4.40 (s, 2H), 6.79 (m, 1H), 6.88 (m, 1H), 7.13 (m, 1H), 7.14 (m, 1H). LRMS (ES+): m/z 190 [MH]+.
References
[1] Patent: WO2006/92731, 2006, A1. Location in patent: Page/Page column 46
spiro<benzofuran-3(2H),4'-piperidine Preparation Products And Raw materials
Raw materials
Preparation Products
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