4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE
- Product Name
- 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE
- CAS No.
- 287952-67-4
- Chemical Name
- 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE
- Synonyms
- Delamanid intermediate;Piperidine, 4-[4-(trifluoroMethoxy)phenoxy]-;4-[4-(TrifluoroMethoxy)phenoxy]piperidine HCl
- CBNumber
- CB31476863
- Molecular Formula
- C12H14F3NO2
- Formula Weight
- 261.24
- MOL File
- 287952-67-4.mol
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Property
- Melting point:
- 71-73℃
- Boiling point:
- 292.2±40.0 °C(Predicted)
- Density
- 1.230±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- form
- powder to crystal
- pka
- 9.65±0.10(Predicted)
- color
- White to Light yellow
- InChI
- InChI=1S/C12H14F3NO2/c13-12(14,15)18-11-3-1-9(2-4-11)17-10-5-7-16-8-6-10/h1-4,10,16H,5-8H2
- InChIKey
- RPQOTFPZKNHYFB-UHFFFAOYSA-N
- SMILES
- N1CCC(OC2=CC=C(OC(F)(F)F)C=C2)CC1
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- MNO000104
- Product name
- 4-[4-(Trifluoromethoxy)phenoxy]piperidine
- Purity
- Aldrich
- Packaging
- 1g
- Price
- $216
- Updated
- 2025/07/31
- Product number
- T3349
- Product name
- 4-[4-(Trifluoromethoxy)phenoxy]piperidine
- Purity
- >97.0%(GC)(T)
- Packaging
- 1g
- Price
- $48
- Updated
- 2025/07/31
- Product number
- T3349
- Product name
- 4-[4-(Trifluoromethoxy)phenoxy]piperidine
- Purity
- >97.0%(GC)(T)
- Packaging
- 5g
- Price
- $235
- Updated
- 2025/07/31
- Product number
- T790890
- Product name
- 4-[4-(Trifluoromethoxy)phenoxy]piperidine
- Packaging
- 5g
- Price
- $415
- Updated
- 2021/12/16
- Product number
- 49059
- Product name
- 4-[4-(Trifluoromethoxy)phenoxy]piperidine
- Packaging
- 1g
- Price
- $625
- Updated
- 2021/12/16
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Chemical Properties,Usage,Production
Uses
4-[4-(Trifluoromethoxy)phenoxy]piperidine is used in the preparation of 3,5-disubstituted isoxazolines as antituberculosis agents.
Synthesis
828-27-3
65214-82-6
287952-67-4
GENERAL STEPS: 9.72 kg of ethyl 4-hydroxypiperidine-1-carboxylate and 10.0 L of triethylamine were dissolved in 15.0 L of toluene and the resulting solution was cooled to below 10 °C. To this solution, 7.07 kg of methanesulfonyl chloride was slowly added dropwise at a temperature below 25 °C, followed by continued stirring for 1 hour at below 25 °C. Next, 5.00 kg of 4-trifluoromethoxyphenol, 10 L of toluene, 17.7 L of 25% aqueous sodium hydroxide and 6.24 kg of 50% aqueous tetra-n-butyl ammonium chloride were added to the reaction solution. The mixture was heated to reflux for 2 hours (internal temperature was maintained at 88°C). After completion of the reaction, the mixture was cooled and the aqueous layer was separated and discarded. The organic layer was washed with 10 L of water. Subsequently, 14.2 kg of potassium hydroxide and 10 L of ethanol were added to the washed organic layer and the mixture was heated to reflux for 4 hours (internal temperature maintained at 98 °C). After cooling, concentration was carried out under reduced pressure. To the concentrated residue, 50 L of toluene was added and the organic layer was washed sequentially with 25 L of water, 25 L of brine and 31 L of aqueous ammonium chloride. The washed toluene solution was concentrated under reduced pressure. The concentrated residue was dissolved in a solvent mixture of 5 L of isopropanol, 50 L of water and 2.5 L of 25% aqueous sodium hydroxide to form a homogeneous solution, which was subsequently cooled to below 10 °C. After the crystals precipitated, stirring was continued below 10 °C for 1 h. The precipitate was then collected by filtration. The crystals were washed with 15 L of water and dried in air to give 6.67 kg of 4-(4-trifluoromethoxyphenoxy)piperidine (isolated yield: 90.9%). 1H-NMR (300 MHz, CDCl3) δ ppm: 1.41 (2H, dddd), 1.90 (2H, m), 2.55 (2H, dddd), 2.92 (2H, dddd), 3.33 (1H, brs), 4.39 (1H, tt), 7.03 (2H, d), 7.25 (2H, d).
References
[1] Patent: US2018/65931, 2018, A1. Location in patent: Paragraph 0135
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE manufacturers
- Product
- 4-[4-(trifluoromethoxy)phenoxy]piperidine 287952-67-4
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1Ton
- Release date
- 2022-09-30
- Product
- 4-(4-Trifluoromethoxyphenoxy)piperidine 287952-67-4
- Price
- US $10.00-15.00/g
- Min. Order
- 10g
- Purity
- 99%
- Supply Ability
- 10t
- Release date
- 2022-09-21
- Product
- 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE 287952-67-4
- Price
- US $9.80/KG
- Min. Order
- 1g
- Purity
- ≥99%
- Supply Ability
- 100kg
- Release date
- 2019-12-26