Syntheses of 5-n-Alkylresorcinol dimethyl ethers and 1,14-Bis(3,5-dimethoxyphenyl) tetradecane via β-keto sulphone intermediates

1973 ◽  
Vol 26 (4) ◽  
pp. 799 ◽  
Author(s):  
JR Cannon ◽  
PK Cheong ◽  
CJ Fallick ◽  
BH Hamilton ◽  
IA McDonald ◽  
...  

Alkylation of 3,5-dimethoxy-α-(methylsulphonyl)acetophenone followed by reduction of the resulting monoalkylated products with zinc and acetic acid afforded the corresponding 5-n-acylresorcinol dimethyl ethers. Hydrogenolysis of 5-n-undecoylresorcinol dimethyl ether, prepared in this way, yielded 5-n-undecylresorcinol dimethyl ether. ��� Alkylation of 1-(methylsulphonyl)alkan-3-ones with 3,5- dimethoxybenzyl bromide gave a mixture of mono- and di-substituted products. Clemmensen reduction of the monosubstituted products afforded 5-n-alkylresorcinol dimethyl ethers directly. ��� These reactions have been adapted to provide two syntheses of 1,14- bis(3,5-dimethoxyphenyl)tetradecane.

2011 ◽  
Vol 704-705 ◽  
pp. 592-595
Author(s):  
Zhong Feng Zhang ◽  
Xian Yan Zhou ◽  
Qing Zhi Ma

Phyllostachys heterocyclabegins to be used for black bamboo with high added value. However, the pyrolysis products were severely wasted. Therefore, the chemical components fromPhyllostachys heterocyclawere identified by TD-GC/MS after concentration. The main constituents of 150°С volatiles were acetic acid (46.75%), carbon disulfide (4.90%), 2-furanmethanol (4.10%), benzofuran, 2,3-dihydro-(3.63%), formic acid (3.27%), 2-propanone, 1-hydroxy-(2.80%), 2-propenoic acid, 2-hydroxyethyl ester (2.64%), dimethyl ether (2.15%), .beta.-pinene (1.84%), camphor (1.71%), etc. The main constituents of 180°С volatiles were acetic acid (20.66%), benzofuran, 2,3-dihydro-(14.49%), furfural (8.86%), formic acid (8.37%), 2-furanmethanol (4.17%), 4h-pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methyl-(3.74%), 2(5h)-furanone (2.83%), 2-propanone, 1-hydroxy-(2.74%), etc. The main components of pyrolysis products of Phyllostachys heterocycla in heat charring could also be used as bioenergy materials, but were not only abundant and healthy to human.


2012 ◽  
Vol 554-556 ◽  
pp. 760-763 ◽  
Author(s):  
Bin Ru ◽  
Xin Bao Li ◽  
Ling Jun Zhu ◽  
Guo Hui Xu ◽  
Yue Ling Gu

Gas-phase methanol carbonylation over HMOR catalyst was investigated for the synthesis of dimethyl ether (DME) and acetic acid (HOAc). The results revealed that the selectivity of DME reached 98% and the methanol conversion was 45% under the reaction temperature of 493K. While, the selectivity of HOAc was 30% and the methanol conversion reached 80% when reaction temperature was increased to 573K. TEM, SEM, XRD, N2 physisorbtion, XPS and TG-DTG measurements were performed to characterize the texture and structure of the catalyst. Serious coking on the catalyst surface significantly limited the utilization of unmodified HMOR catalyst in the reaction.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


2001 ◽  
Vol 120 (5) ◽  
pp. A153-A153
Author(s):  
S MIYAMOTO ◽  
K KATO ◽  
Y ISHII ◽  
S ASAI ◽  
T NAGAISHI ◽  
...  

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