CAS: 583-48-2; 3,4-Dimethylhexane

📜3,4-二甲基己烷-3,4-二醇置于nickel(II) Oxide,Aluminum Oxide,氢气体系中,250.0~260.0 °C,9.81 Mpa 条件下,反应生成 3,4-二甲基己烷
参考文献:Schmerling; Friedman; Ipatieff,Journal Of The American Chemical Society,1940,Vol. 62,P. 2448
标题:Schmerling; Friedman; Ipatieff,Journal Of The American Chemical Society,1940,Vol. 62,P. 2448

专利信息

专利号:WO-2013138200-A1
优先权日:2012-03-13
标 题 :Green chemistry synthesis of the malaria drug amodiaquine and analogs thereof
发明人：FORTUNAK JOSEPH MARIAN; KULKARNI AMOL ANANT; KING CHRISTOPHER
权利人:UNIV HOWARD
摘要:Methods are provided for a green chemistry one-pot synthesis of amodiaquine and amodiaquine analogs. The methods have a lower environmental impact, lower investment cost, reduced amounts of byproducts and impurities, and a shorter synthesis time, compared to current conventional synthesis methods. The methods reduce the total number of steps in the synthesis from four to five down to two, thereby simplifying production; and allow a reduced number of solvents and reagents to be used in production, thereby reducing the waste generated in the synthesis. The methods can reduce the waste to about 3-5 kilograms of waste generated per kilogram of product produced; and surprisingly improve the overall yield from 60-65% to greater than 90% as compared to the current conventional synthesis methods for amodiaquine and its analogs.

专利号:US-2003162992-A1
优先权日:2001-12-14
标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
发明人：WATANABE KYOICHI A; DU JINFA
摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.

专利号:WO-2011000934-A1
优先权日:2009-07-02
标 题 :Enabling synthesis of speech having a target characteristic
发明人：YAMAGISHI JUNICHI; KING SIMON ALISTAIR; RENALS STEPHEN JOHN
权利人:UNIV COURT OF THE UNVIERSITY OF EDINBURGH; YAMAGISHI JUNICHI; KING SIMON ALISTAIR; RENALS STEPHEN JOHN
摘要:A method involving: inputting target speech features derived from speech having a target characteristic; inputting labelling of the speech; and adapting, using a speech feature transform, statistical parameters of a predefined statistical parametric speech model to create an adapted statistical parametric speech model configured to synthesis speech having the target characteristic.

专利号:WO-2015183067-A1
优先权日:2014-05-30
标题 :Synthesis of analogues of y-amino acids and resulting products
发明人：FERNÃ?NDEZ ZERTUCHE MARIO; TOVAR GUDIÑO ERIKA; TRUJILLO FERRARA JOSÉ GUADALUPE; GUEVARA SALAZAR JUAN ALBERTO
权利人:UNIV AUTÓNOMA DEL ESTADO DE MORELOS
摘要:The invention relates to a compound of formula (see formula), suitable for use as drugs in the treatment of chronic neurodegenerative disorders of the Huntington's disease, Parkinson's disease and epilepsy type, inter alia . The invention relates to novel methods for the synthesis of said analogues and the pharmaceutically acceptable solvates and salts thereof.

专利号:WO-2013144924-A1
优先权日:2012-03-29
标 题:An improved process for the synthesis of strobilurin fungicides viz trifloxystrobin and kresoxim-methyl
发明人：KAMARAJ PASUMPON; SATAM VIJAY SHRIKANT; AJJANNA MAHALINGAPPA SRIDHARA; NANDI TAPASKUMAR; BOBADE ANNA; SHINDE RAVINDRA; NAIK PARAG; MOHITE DHANAJI; KADAM SUBHASH; HINDUPUR RAMA MOHAN; PATI HARI NARAYAN; MANE AVINASH; VADIRAJ SUPHALA GOPINATH; VENKATESH PRABHU MOODBIDRI
权利人:RALLIS INDIA LTD
摘要:The present invention relates to an improved process for the synthesis of E -isomer of compound of formula (5). It further relates to the conversion of formula (5), wherein R is H, to Intermediate (I) and subsequently to substantially pure Trifloxystrobin, compound of formula (I) in good yield.

专利号:US-10597340-B2
优先权日:2013-05-10
标 题:Synthesis of fluorinated radiopharmaceuticals via electrochemical fluorination
发明人：SADEGHI SAMAN; HE QINGGANG; LEBEDEV ARTEM
权利人:UNIV CALIFORNIA
摘要:Provided herein are methods and compositions for the electrochemical selective radiofluorination of aromatic molecules. The resulting fluorine-18 labeled compounds are ideal radionuclides for use in Positron Emission Tomography (PET); they are also difficult to radiolabel efficiently and with high specific activity using existing approaches. For example, radiopharmaceuticals such as [F18]L-DOPA, which is indispensable in PET brain disease imaging, may be made electrochemically with high radiochemical yield and high specific activity using 18F-. The invention process described herein opens new possibilities and provides wider access to PET tracers such as 18F-L-Dopa, since 18F- is much more widely available than the 18F 2 , currently used for synthesis of electron rich substrates.