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3973-62-4

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3973-62-4 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 3973-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3973-62:
(6*3)+(5*9)+(4*7)+(3*3)+(2*6)+(1*2)=114
114 % 10 = 4
So 3973-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N/c1-2-5-10(6-3-1)11-7-4-8-12-9-11/h10-12H,1-9H2/p+1/t11-/m1/s1

3973-62-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Phenylpiperidine

1.2 Other means of identification

Product number -
Other names Piperidine, 3-phenyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3973-62-4 SDS

3973-62-4Synthetic route

3-phenylpyridine
1008-88-4

3-phenylpyridine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With hydrogen In water at 140℃; under 45004.5 Torr; for 24h; Autoclave; chemoselective reaction;98%
With triphenylborane; diphenylsilane; diphenylamine In toluene at 110℃; for 24h; Glovebox; Inert atmosphere; chemoselective reaction;90%
With palladium diacetate; C3H6BNO2 In tetrahydrofuran at 60℃; for 24h; Schlenk technique; Inert atmosphere;87.3%
N-benzyl-3-phenylpiperidine
3979-67-7

N-benzyl-3-phenylpiperidine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With 18 % Pd/C; hydrogen; acetic acid In ethanol at 60℃; under 760.051 Torr; for 12h;89.3%
N-benzyl-5-phenyl-1,2,3,6-tetrahydropyridine

N-benzyl-5-phenyl-1,2,3,6-tetrahydropyridine

A

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

B

N-benzyl-3-phenylpiperidine
3979-67-7

N-benzyl-3-phenylpiperidine

Conditions
ConditionsYield
With palladium on activated charcoal Hydrogenation;
5-phenylpiperidin-2-one
3973-63-5

5-phenylpiperidin-2-one

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With sodium tetrahydroborate; boron trifluoride diethyl etherate In tetrahydrofuran 1) r.t., 2 h, 2) reflux, 2 h; Yield given;
(+-)-1-benzyl-3-phenyl-piperidine

(+-)-1-benzyl-3-phenyl-piperidine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With palladium on activated charcoal; ethanol Hydrogenation;
(+-)-2-phenyl-glutaronitrile

(+-)-2-phenyl-glutaronitrile

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With sodium; butan-1-ol
(+-)-3-acetoxy-1-benzyl-3-phenyl-piperidine

(+-)-3-acetoxy-1-benzyl-3-phenyl-piperidine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With palladium on activated charcoal; ethanol Hydrogenation;
(+-)-3-phenyl-piperidine-2,6-dione

(+-)-3-phenyl-piperidine-2,6-dione

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With lithium aluminium tetrahydride; diethyl ether
(+-)-5-phenoxy-2-phenyl-pentylamine

(+-)-5-phenoxy-2-phenyl-pentylamine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With hydrogen bromide anschliessend Erhitzen in Toluol mit wss. Natronlauge;
(+-)-5-phenyl-piperidin-2-one

(+-)-5-phenyl-piperidin-2-one

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With sodium; butan-1-ol
1,4-dioxane
123-91-1

1,4-dioxane

γ-cyano-γ-phenylpimelonitrile
16320-20-0

γ-cyano-γ-phenylpimelonitrile

copper oxide-chromium oxide catalyst

copper oxide-chromium oxide catalyst

A

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

B

5-phenyl-1-aza-bicyclo[3.3.1]nonane
37179-27-4

5-phenyl-1-aza-bicyclo[3.3.1]nonane

C

-base C14H18N2(?)

-base C14H18N2(?)

D

amine of mp: 247

amine of mp: 247

Conditions
ConditionsYield
at 230℃; under 128714 Torr; Hydrogenation;
1-methanesulfonyl-3-phenyl-piperidine
906360-17-6

1-methanesulfonyl-3-phenyl-piperidine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With sodium amalgam; sodium phosphate In methanol at 20℃; for 2h;
3-phenyl-1-p-toluenesulfonylpiperidine
906360-21-2

3-phenyl-1-p-toluenesulfonylpiperidine

3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
With sodium amalgam; sodium phosphate In methanol at 20℃; for 2h;
3-phenylpiperidine
3973-62-4

3-phenylpiperidine

Conditions
ConditionsYield
Stage #1: 1-methyl-3-phenylpiperidine With carbonochloridic acid 1-chloro-ethyl ester; sodium carbonate In 1,2-dichloro-ethane at 70℃; for 1h;
Stage #2: In methanol; 1,2-dichloro-ethane at 70℃; for 1h;

3973-62-4Relevant articles and documents

Method for preparing piperidine compound by reducing pyridine compound through hydrogen transfer

-

Paragraph 0027; 0028; 0029; 0030; 0031, (2021/04/28)

The invention discloses a method for preparing a piperazine compound through a hydrogen transfer reduction of a pyridine compound, belonging to the field of organic synthesis. Under mild conditions, pyridine derivatives are used as raw materials, oxazolidine is used as a hydrogen transfer reagent, and cheap transition metals such as copper, cobalt, silver, palladium and the like are used as catalysts for catalysis of a hydrogen transfer reaction on 1,2,3,4-substitution sites, so a series of hydrogen transfer reduction product piperidine compounds are prepared, wherein the oxazaborolidine is obtained by a reaction of amino acid with a tetrahydrofuran complex of borane. The method has the advantages that product yield is high, reaction conditions are mild, the general applicability of raw materials is good, a hydrogen transfer reagent is cheap and easy to obtain, and good reproducibility can still be shown after quantitative reaction is conudcted. Therefore, the method of the invention provides an effective scheme for the industrial production of other high-value compounds containing the structure in the future.

Construction of azacycles by intramolecular amination of organoboronates and organobis(boronates)

Xu, Peilin,Zhang, Mingkai,Ingoglia, Bryan,Allais, Christophe,Dechert-Schmitt, Anne-Marie R.,Singer, Robert A.,Morken, James P.

supporting information, p. 3379 - 3383 (2021/05/10)

Intramolecular amination of organoboronates occurs with a 1,2-metalate shift of an aminoboron ate complex to form azetidines, pyrrolidines, and piperidines. Bis(boronates) undergo site-selective amination to form boronate-containing azacycles. Enantiomerically enriched azacycles are formed with high stereospecificity.

Hydrogenation of Pyridines Using a Nitrogen-Modified Titania-Supported Cobalt Catalyst

Chen, Feng,Li, Wu,Sahoo, Basudev,Kreyenschulte, Carsten,Agostini, Giovanni,Lund, Henrik,Junge, Kathrin,Beller, Matthias

supporting information, p. 14488 - 14492 (2018/10/26)

Novel heterogeneous catalysts were prepared by impregnation of titania with a solution of cobalt acetate/melamine and subsequent pyrolysis. The resulting materials show an unusual nitrogen-modified titanium structure through partial implementation of nitrogen into the support. The optimal catalyst displayed good activity and selectivity for challenging pyridine hydrogenation under acid free conditions in water as solvent.

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