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HERO ID
8177209
Reference Type
Journal Article
Title
Organophosphorus Synthesis Without Phosphorus Trichloride: The Case for the Hypophosphorous Pathway
Author(s)
Montchamp, J
Year
2013
Is Peer Reviewed?
1
Journal
Phosphorus, Sulfur, and Silicon and the Related Elements
ISSN:
1042-6507
EISSN:
1563-5325
Publisher
TAYLOR & FRANCIS LTD
Location
ABINGDON
Volume
188
Issue
1-3
Page Numbers
66-75
Language
English
DOI
10.1080/10426507.2012.727925
Web of Science Id
WOS:000319042300025
Abstract
The vast majority of organophosphorus compounds is currently synthesized from phosphorus trichloride (PCl3), even though the final consumer products do not contain reactive phosphorus-chlorine bonds. In order to bypass phosphorus trichloride, significant interest has been devoted to functionalizing elemental phosphorus (P4, the precursor to PCl3), red phosphorus (Pred), or phosphine (PH3). Yet, other industrial-scale precursors are hypophosphorous derivatives (H 3PO2 and its alkali salts), but their use as phosphorus trichloride replacements has been completely overlooked. Here, the case is made for an alternative approach to the industrial synthesis of organophosphorus compounds based on hypophosphites. © 2013 Copyright Taylor and Francis Group, LLC.
Keywords
Hypophosphite; H-phosphinic acid; phosphonic acid; phosphorus trichloride; elemental phosphorus; phosphine
Conference Name
19th International Conference on Phosphorus Chemistry (ICPC)
Conference Location
Rotterdam, NETHERLANDS
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