[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide
[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Basic information
- Product Name:
- [1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide
- Synonyms:
-
- [1-(ETHOXYCARBONYL)ETHYL]TRIPHENYL PHOSPHONIUM BROMIDE, 95+%
- (1-ETHOXYCARBONYLETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
- 1-CARBETHOXYETHYL TRIPHENYLPHOSPHONIUM BROMIDE
- (2-ethoxy-1-methyl-2-oxoethyl)triphenylphosphonium bromide
- carbethoxy Ethyl Triphenyl Phosphonium Bromide
- (1-ETHOXYCARBONYLETHYL)TRIPHENYLPHOSPHONIUM BROMIDE 96%
- 1-Carbethoxyethyl triphenylphosphonium bromide 98%
- (1-carboethoxyethyl)triphenylphosphonium bromide
- CAS:
- 30018-16-7
- MF:
- C23H24BrO2P
- MW:
- 443.32
- EINECS:
- 250-002-2
- Product Categories:
-
- Isoquinolines ,Quinolines ,Quinazolines ,Quinaldines
- Mol File:
- 30018-16-7.mol
[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Chemical Properties
- Melting point:
- 152 °C
- storage temp.
- Refrigerator (+4°C)
- solubility
- Chloroform, Methanol
- form
- Solid
- color
- Pale Yellow
- Water Solubility
- soluble
- Sensitive
- Hygroscopic
- BRN
- 3822244
- InChI
- InChI=1S/C23H24O2P.BrH/c1-3-25-23(24)19(2)26(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22;/h4-19H,3H2,1-2H3;1H/q+1;/p-1
- InChIKey
- RSYXORMKBUFAMS-UHFFFAOYSA-M
- SMILES
- [P+](C1C=CC=CC=1)(C1C=CC=CC=1)(C1C=CC=CC=1)C(C)C(=O)OCC.[Br-]
- CAS DataBase Reference
- 30018-16-7(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-29-22
- Safety Statements
- 26-36-8-37/39
- Hazard Note
- Irritant/Hygroscopic
- HS Code
- 29310099
MSDS
- Language:English Provider:ALFA
[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
suzuki reaction
Uses
1-Ethoxycarbonylethyl)triphenylphosphonium bromide is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is widely used as an organophosphine catalyst.
Synthesis
603-35-0
535-11-5
30018-16-7
1.0 g of triphenylphosphine was dissolved in 15 mL of ethyl acetate and 0.55 mL of ethyl 2-bromopropionate was added to this solution. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the bulk of the resulting white solid product was collected by diafiltration. The solids were washed with ethyl acetate to give a final 1.35 g of white solid product ethoxycarbonyl ethyltriphenylphosphonium bromide in 80.5% yield.
References
[1] European Journal of Organic Chemistry, 2016, vol. 2016, # 12, p. 2110 - 2114
[2] Chemistry - A European Journal, 2015, vol. 21, # 20, p. 7408 - 7412
[3] Tetrahedron, 2010, vol. 66, # 26, p. 4745 - 4759
[4] Journal of Organic Chemistry, 1984, vol. 49, # 22, p. 4293 - 4295
[5] Patent: CN103864753, 2016, B. Location in patent: Paragraph 0087; 0110-0111
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[1-(Ethoxycarbonyl)ethyl]triphenylphosphonium bromide(30018-16-7)Related Product Information
- Ethyl acetate
- Ethyltriphenylphosphonium bromide
- Triphenylphosphine oxide
- 2-Ethoxyethanol
- 2-Ethoxyphenol
- Ethylparaben
- Ethoxyquin
- Clidinium bromide
- Sodium bromate
- Ethyltriphenylphosphonium acetate
- Diphenylphosphine
- Ethanol
- Ethidium bromide
- Chlorodiphenylphosphine
- Tetraethylammonium bromide
- DIETHOXYMETHANE
- Diethoxymethyl acetate
- Ethyl acrylate