FIELD: chemistry.
SUBSTANCE: method includes reacting symmetrical acetylenes with triethylaluminium in the presence of a zirconocene dichloride catalyst (Cp2ZrCl2) in toluene in an argon atmosphere at 20-40°C and atmospheric pressure for 4-12 hours, followed by addition to the reaction mass at (-5) to (-10)°C of phenyl- or alkyl dichlorophosphine, taken in equimolar ratio to Et3Al, and mixing at room temperature for 10-30 minutes. The output of the end product after hydrolysis of the reaction mass is 38-92%.
EFFECT: high output of the end product.
1 tbl, 1 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF PRODUCING 2,3-DIALKYL-1-PHENYL(ALKYL)SUBSTITUTED PHOSPHOL-2-ENE-1-SULPHIDES | 2014 |
|
RU2556008C1 |
METHOD OF PRODUCING 2,3-DIALKYL-1-PHENYL(ALKYL)SUBSTITUTED PHOSPHOL-2-ENE-1-OXIDES | 2014 |
|
RU2570205C2 |
METHOD OF COMBINED PREPARATION OF 1-(DIALKYLAMINE)- 2,3,4,5-TETRAALKYL (ARYL) ALUMACYCLOPENTADIENES AND 1- (DIALKYLAMINE)-2,3-DIALKYL(ARYL) ALUMACYCLOPROPENES | 1997 |
|
RU2131432C1 |
METHOD OF COMBINED PREPARATION OF 1-(ALKOXY)-2,3,4,5- TETRAALKYL-(ARYL) ALUMACYCLOPENTADIENES AND 1-(ALKOXY)- 2,3-DIALKYL (ARYL)ALUMACYCLOPROPENES | 1997 |
|
RU2130024C1 |
METHOD OF SYNTHESIS OF 1,2-DIALKYL-1Z,3-BUTADIENES | 2000 |
|
RU2185360C1 |
METHOD FOR PREPARING 1,7,8,9-TETRAALKYL-10-ETHYL-4-OXO-10-ALUMINATRICYCLO[5,2,1,0]-DEC-8-ENE-3,5-DIONES | 2004 |
|
RU2275374C2 |
METHOD OF COMBINED SYNTHESIS OF 1-(ALKOXY)-2,4-DIALKYL(PHENYL)- -ALUMACYCLOPENTADIENS AND 1-(ALKOXY)-2-ALKYL(PHENYL)ALUMA- -CYCLOPROPENES | 1997 |
|
RU2131431C1 |
METHOD FOR PREPARING 10-CHLORO-1,7,8,9-TETRAALKYL-4-METHYL-4-AZA-10-ALUMINATRICYCLO[5.2.1.0]DEC-8-ENE-3,5-DIONES | 2005 |
|
RU2295529C1 |
METHOD FOR PREPARING 11-CHLORO-1,8,9,10-TETRAALKYL-11-ALUMINATRICYCLO[6.2.1.0]UNDEC-9-ENE-3,6-DIONES | 2005 |
|
RU2295530C1 |
METHOD OF PREPARING 4,5-DIALKYL (PHENYL) 1 | 1995 |
|
RU2145319C1 |
Authors
Dates
2015-07-10—Published
2014-04-04—Filed