Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Phosphorus halide >  (tert-Butoxycarbonylmethyl)triphenylphosphanium bromide

(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide

Basic information Safety Supplier Related

(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide Basic information

Product Name:
(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide
Synonyms:
  • [2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]-triphenylphosphonium bromide
  • tert-Butoxycarbonylmethyltriphenylphosphoniumbrom
  • (tert-Butoxycarbonylmethyl)tripheenyphosphonium bromide
  • (TERT-BUTOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
  • carbo-tert-butoxymethyl triphenylphosphonium bromide
  • (tert-Butoxycarbonylmethyl)triphenylphosphanium bromide
  • (tert-Butoxycarbonylmethyl)triphenylphosphonium bromide, 98 %
  • carbo-tert-butoxymethyl triphenylphosp
CAS:
59159-39-6
MF:
C24H26BrO2P
MW:
457.34
Product Categories:
  • C-C Bond Formation
  • Olefination
  • Wittig Reagents
Mol File:
59159-39-6.mol
More
Less

(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide Chemical Properties

Melting point:
178 °C (dec.)(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
BRN 
4631405
CAS DataBase Reference
59159-39-6(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29319019

MSDS

More
Less

(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide Usage And Synthesis

Uses

Reactant for:

  • Rhodium-catalyzed asymmetric hydrogenation reactions
  • Wittig reaction
  • Wittig methylenation
  • Preparation of N-(phenylmethyl)-cis-pyrrolidinediacetic acid esters via double aza-Michael addition reaction
  • Stereoselective preparation of of α-fluoro-α,β-unsaturated esters via deprotonation, followed by fluorination and stereoselective Wittig olefination with aldehydes
  • Wittig chain extension reactions

reaction suitability

reaction type: C-C Bond Formation

Synthesis

5292-43-3

603-35-0

59159-39-6

Example 3: The general procedure for the synthesis of (tert-butoxycarbonylmethyl)triphenylphosphonium bromide from tert-butyl bromoacetate and triphenylphosphine is as follows: In another embodiment, the functionalized lactone comprises a carboxylate protecting group as shown in Fig. 1. 10. Ylide synthesis was carried out using the following reagents and conditions: (a) triphenylphosphine (PPh3), benzene (C6H6), reaction time 12 h at room temperature (rt); (b) 20% aqueous sodium hydroxide solution (NaOH, aq), reaction time 5 h at room temperature.

References

[1] Patent: US2007/265243, 2007, A1. Location in patent: Page/Page column 4
[2] Bioorganic and Medicinal Chemistry, 2001, vol. 9, # 1, p. 199 - 209
[3] Phosphorus, Sulfur and Silicon and the Related Elements, 2008, vol. 183, # 5, p. 1188 - 1208
[4] Patent: US2007/43088, 2007, A1. Location in patent: Page/Page column 5
[5] Organic Process Research and Development, 2009, vol. 13, # 4, p. 710 - 715

(tert-Butoxycarbonylmethyl)triphenylphosphanium bromideSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com