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三乙胺

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The results indicate that the optimized sulfonylation reaction time is 4 h, the materiel rate of chlorosulfonic acid and 2-chloroimidazo[1,2-α]pyridine is 1.2 : 1, with ethylamine the yield increasing from 15.4% to above 70%; the optimized ammonolysis reaction time is 3 h and the reaction temperature is 27℃, with the acetonitrile yield increasing from 60.1% to above 79.6%.

实验结果表明,磺酰化反应的最佳反应时间为4 h,氯磺酸与2-氯咪唑并[1,-α]吡啶的用量比为1.2:1,加入三乙胺可将收率由15.4%提高到70%以上;氨解反应的最佳反应时间为3 h,反应温度为27 ℃,加入乙腈可将收率由60.1%提高到79.6%;方案经改进后,总反应时间缩短3 h,收率提高了5.5%。

Some materials were synthesized in this paper at first, 1-nitro-2-pentanol was synthesized with nitromathane and butyraldehyde and the yield was 70.2%; l-nitro-2-pentanol was reduced to 1 -amino-2- pentanol with iron and the yield was 65.2%.

分别用氢氧化钠、三乙胺为缚酸剂,2-氨基-1-丁醇、1-氨基-2-戊醇、环己酮和二氯乙酰氯为原料,采用一步法和分步法合成了两种潜在除草剂安全剂。

Methods:A YWG-C18 column was used.The mobile phase consist ed of acetonitrile containing 0.2% methanol-water solution containing 0.1% tri ethylamine and 0.1% phosphoric acid(3∶97)and the detection wavelength was 220 nm.

采用高效液相色谱法,色谱柱为YWG-C18柱,流动相为0.2%甲醇的乙腈溶液-含0.1%三乙胺、0.1%磷酸的水溶液(3∶97),检测波长为220 nm。

On the basis of insoluble hydantoin bactericide prepared,the hydrophilic groups,such as trimethylamine group and triethylamine group,were introduced to the loading resin,such as chloromethyl polystyrene and formyl polystyrene.

在制成水不溶性海因类杀菌剂的基础上,在其载体树脂如氯球和醛基树脂上引入亲水基,如三甲胺基或三乙胺基。

The better technology has been obtained: taking water-EG as solvent 2-imidazolidinone was prepared. The molar ratio of the methanal (36%) to the formic acid (85%) is 1:2.8, reaction temperature is 95~100℃, reaction time is 16 h, taking cuprous chloride and triethylamine as catalyst, the molar ratio of the cuprous chloride and triethylamin to 2-imidazolidinone is 1.0% while 1,3-DMI was prepared.

较佳工艺条件为:制备2-咪唑啉酮时,以水-乙二醇混合作溶剂;制备1,3-DMI时,甲醛(36%):甲酸(85%)摩尔比为1:2.8,反应温度95~100℃,反应时间16 h,氯化亚铜和三乙胺作催化剂,用量分别是2-咪唑啉酮摩尔数的1.0%。

The synthesis of vitamin E oleate by using vitamin E and oleic acid was studied.

以维生素E及油酸为原料,乙酸酐为共反应剂,三乙胺为催化剂合成了维生素E 油酸酯。

Through orthogonal experiment,the reaction was carried out in acetate anhydride co-reagent and triethylamine as catalyst.

以维生素E及油酸为原料,乙酸酐为共反应剂,三乙胺为催化剂合成了维生素E油酸酯。

The first step is conducted at a pH in the range of about 4.5-9.5, employing the combination of a hexaalkylguanidinium salt as a phase transfer catalyst and a tertiary amine such as triethylamine.

第一步骤是在pH值为约4.5―9.5的范围内进行的,使用作为相转换催化剂的六烷基__盐和叔胺如三乙胺的混合物。

Two compounds were synthesized with two methods. The two compounds can be synthesized by two steps with triethylamine as catalyst.

分别用氢氧化钠、三乙胺为缚酸剂,3-氨基-2-丁醇、2-氨基-3-戊醇、环己酮和二氯乙酰氯为原料,采用一步法和分步法合成了两种潜在除草剂安全剂。

The title compounds were synthesized by the reaction of symmetric N , N '-diarylthioureas with hexylamine in the presence of triethyl amine,and the intermediate N , N '-diarylthioureas were formed by the direct reaction of carbon disulfide and arylamines.

首先采用二硫化碳与胺直接反应得到对称的N, N'-二芳基硫脲,然后在三乙胺存在下与环己胺反应得到1-环己基-3-芳基硫脲。产物结构经核磁共振和质谱分析确证

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