SYNTHESIS OF BUTYRONITRILE VIA AMMONOLYSIS OF BUTYLALCOHOL AND DEHYDROGENATION OF BUTYLAMINE OVER MO2N

被引:15
作者
ABE, H [1 ]
BELL, AT [1 ]
机构
[1] UNIV CALIF BERKELEY,DEPT CHEM ENGN,BERKELEY,CA 94720
关键词
D O I
10.1006/jcat.1993.1220
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Investigations were carried out of the synthesis of butyronitrile via the ammonolysis of butylalcohol and the dehydrogenation of butylamine aver Mo2N. At 573 K butyronitrile is produced with virtually 100% yield by both reactions. The ammonolysis of butyalcohol proceeds via dehydrogenation of the butylalcohol to form butyraldehyde, which then reacts with ammonia to produce butylimine. Butyronitrile is formed by butylimine dehydrogenation. The formation of butyronitrile from butylamine occurs via the stepwise dehydrogenation of the amine. The presence of ammonia in the gas phase suppresses the hydrogenolysis of either butylalcohol or bulylamine. © 1993 Academic Press, Inc.
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页码:430 / 436
页数:7
相关论文
共 11 条
[1]  
Autorenkollektiv, 1977, ORGANIKUM
[2]  
Bashkirov A. N., 1987, NEFTEKHIMIYA, V27, P818
[3]   GAS-PHASE SYNTHESIS OF NITRILES [J].
CARD, RJ ;
SCHMITT, JL .
JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (04) :754-757
[4]  
Habermann C.E., 1979, US Patent, Patent No. [4152353 A, 4152353]
[5]  
Johnson R.W., 1989, FATTY ACIDS IND
[6]  
KORCHAGOVA EK, 1982, ZH PRIKL KHIM, V55, P2784
[7]   HYDRODENITROGENATION OF QUINOLINE OVER HIGH-SURFACE-AREA MO2N [J].
LEE, KS ;
ABE, H ;
REIMER, JA ;
BELL, AT .
JOURNAL OF CATALYSIS, 1993, 139 (01) :34-40
[8]  
MARKIEWITZ KH, 1966, Patent No. 3278598
[9]  
PATTISON ES, 1968, FATTY ACIDS THEIR IN
[10]  
TANABE K, 1989, NEW SOLID ACIDS BASE