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Title: Substituted dipyrromethanes and their preparation

Abstract

New chemical compounds, bis(pyrrol-2-yl)halocarbylmethanes, also known as meso-halocarbyl dipyrromethanes, are made by reacting pyrrole in either of two reaction schemes. One such scheme converts pyrrole through an intermediate, a halocarbyl carbonyl pyrrole, to a [2-(1-hydroxyl-1-hydro1-halocarbyl)pyrrole], and then converts the latter to the desired halocarbyldipyrromethane; the last step in this scheme is a novel and useful method in itself. The other such sequence converts pyrrole, by reaction with a halocarbyl aldehyde, directly to the desired halocarbyl dipyrromethane.

Inventors:
Issue Date:
Research Org.:
Sun Refining and Marketing Company
OSTI Identifier:
264563
Patent Number(s):
5,536,844
Application Number:
PAN: 8-562,776
Assignee:
SunCompany, Inc., Philadelphia, PA (United States)
DOE Contract Number:  
FC21-90MC26029
Resource Type:
Patent
Resource Relation:
Other Information: PBD: 16 Jul 1996
Country of Publication:
United States
Language:
English
Subject:
40 CHEMISTRY; PYRROLES; CHEMICAL PREPARATION; CHEMICAL REACTIONS; ALDEHYDES; ALKANES; REACTION INTERMEDIATES; ORGANIC HALOGEN COMPOUNDS; CARBONYLS

Citation Formats

Wijesekera, T. Substituted dipyrromethanes and their preparation. United States: N. p., 1996. Web.
Wijesekera, T. Substituted dipyrromethanes and their preparation. United States.
Wijesekera, T. Tue . "Substituted dipyrromethanes and their preparation". United States.
@article{osti_264563,
title = {Substituted dipyrromethanes and their preparation},
author = {Wijesekera, T},
abstractNote = {New chemical compounds, bis(pyrrol-2-yl)halocarbylmethanes, also known as meso-halocarbyl dipyrromethanes, are made by reacting pyrrole in either of two reaction schemes. One such scheme converts pyrrole through an intermediate, a halocarbyl carbonyl pyrrole, to a [2-(1-hydroxyl-1-hydro1-halocarbyl)pyrrole], and then converts the latter to the desired halocarbyldipyrromethane; the last step in this scheme is a novel and useful method in itself. The other such sequence converts pyrrole, by reaction with a halocarbyl aldehyde, directly to the desired halocarbyl dipyrromethane.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1996},
month = {7}
}