(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide
(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
(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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
(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
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(tert-Butoxycarbonylmethyl)triphenylphosphanium bromide(59159-39-6)Related Product Information
- Ethidium bromide
- tert-Butanol
- Tetrabutylammonium bromide
- Rocuronium bromide
- Allyl bromide
- Sodium bromate
- Sodium bromide
- Tetrabutyl titanate
- Chlorodimethylphenylsilane
- Methylmagnesium Bromide
- Potassium bromide
- Methyl bromide
- Methyltriphenylphosphonium bromide
- (2-HYDROXYETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
- (Carbomethoxymethyl)triphenylphosphonium bromide
- (Carbethoxymethyl)triphenylphosphonium bromide
- CARBOXYMETHYL DIPHENYLPHOSPHINE OXIDE
- (ETHOXYCARBONYLMETHYL)DIPHENYLPHOSPHINE