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Merck
모든 사진(1)

주요 문서

90827

Sigma-Aldrich

Tributylphosphine

≥93.5% (Tri-N-butylphosphine, GC)

동의어(들):

P(n-Bu)3, TBP

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About This Item

Linear Formula:
[CH3(CH2)3]3P
CAS Number:
Molecular Weight:
202.32
Beilstein:
1738261
EC Number:
MDL number:
UNSPSC 코드:
12352128
PubChem Substance ID:
NACRES:
NA.22

vapor density

9 (vs air)

Quality Level

분석

≥93.5% (Tri-N-butylphosphine, GC)
≥97% (Tri-N-butylphospine + isomers)

형태

liquid

autoignition temp.

392 °F

반응 적합성

reaction type: Acetylations
reagent type: ligand

refractive index

n20/D 1.462 (lit.)
n20/D 1.463

bp

150 °C/50 mmHg (lit.)

density

0.81 g/mL at 25 °C (lit.)

작용기

phosphine

SMILES string

CCCCP(CCCC)CCCC

InChI

1S/C12H27P/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-12H2,1-3H3

InChI key

TUQOTMZNTHZOKS-UHFFFAOYSA-N

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일반 설명

Tributylphosphine (TBP) is a potential nucleophile. It acts as a weak base in organic solvents. It is an important catalyst for the acylation reactions. It is an efficient promoting reagent for the ring-opening reaction of various epoxides and aziridines. TBP in conjugation with 1,1′-(azodicarbonyl)dipiperidine (ADDP) constitutes Mitsunobu reagent. This reactive phosphine allows the formation of a strained lactone.

애플리케이션

Tributylphosphine was used in the preparation of silver nanoparticles (AgNPs) functionalized with an organometallic bifunctional thiol containing Pt(II) centers.
It may be used in the following processes:
  • As reducing agent for alkyl disulfides and aromatic disulfides.
  • As catalyst for the synthesis of 2-substituted 1,3-benzoselenazoles.
  • As promoter for the ring opening of epoxides and aziridines with nucleophiles.
  • As a reagent in the preparation of 6-substituted penicillanate esters by reduction of 6-bromo-6-substituted penicillanate esters in high diastereoselectivity.
  • As a catalyst in the acylation reaction of alcohols.
  • As a catalyst to prepare rotaxanes by the acylation of corresponding pseudorotaxanes using 3,5-dimethylbenzoic anhydride.
  • As a catalyst to prepare vinyl thioethers by the Michael addition of ethanethiol to various alkynyl ketones.
  • As a promoter in the conjugate addition of non-nucleophilic N-containing compounds with Michael acceptors.

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1A

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 2

Flash Point (°F)

242.6 °F - closed cup

Flash Point (°C)

117 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

이미 열람한 고객

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Tributylphosphine, excellent organocatalyst for conjugate additions of non-nucleophilic N-containing compounds.
Gimbert C, et al.
Tetrahedron, 63(34), 8305-8310 (2007)
Tributylphosphine-catalyzed reaction of ethanethiol with alkynyl ketones.
Zhao S, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 22(4), 397-400 (2011)
N. Rehnberg, G. Magnusson
The Journal of Organic Chemistry, 55, 5467-5467 (1990)
A.B. Smith III et al.
Journal of the American Chemical Society, 114, 2567-2567 (1992)
Synthesis of 2-Substituted 1, 3-Benzoselenazoles from Carboxylic Acids Promoted by Tributylphosphine.
Schwartz Radatz C, et al.
European Journal of Organic Chemistry, 31, 6945-6952 (2014)

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