CN108084069B - 一种硫醇水相氧化制备二硫醚的方法 - Google Patents

一种硫醇水相氧化制备二硫醚的方法 Download PDF

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CN108084069B
CN108084069B CN201711121966.0A CN201711121966A CN108084069B CN 108084069 B CN108084069 B CN 108084069B CN 201711121966 A CN201711121966 A CN 201711121966A CN 108084069 B CN108084069 B CN 108084069B
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张俊杰
蒋婷婷
王曦
麦裕良
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Dongdai Jinan Intelligent Technology Co ltd
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Abstract

本发明公开了一种硫醇水相氧化制备二硫醚的方法,包括以下步骤:有氧条件下,将催化剂加入硫醇水溶液中,20~100℃反应2~120min,得到二硫醚。本发明在水相中进行反应,以空气为氧化剂,无需使用有机溶剂,产物收率高,反应条件温和,反应过程绿色环保,生产成本低,适合大面积推广使用。

Description

一种硫醇水相氧化制备二硫醚的方法
技术领域
本发明涉及一种硫醇水相氧化制备二硫醚的方法。
背景技术
二硫醚是一类重要的有机硫化合物,用途十分广泛,例如:1)用作有机合成反应中的保护基团;2)用作硫化剂制备橡胶和弹性体;3)用于合成农药、饲料添加剂、香料香精等;4)作为关键中间体合成亚磺酰基化合物、硫基化合物和含硫杂环化合物。传统的方法在制备二硫醚的过程中需要使用大量的氧化剂和催化剂,如铈(IV)盐、高锰酸盐、过渡金属氧化物、过氧化物、氯化铁、氯酸钠、氧化亚氮和卤族元素等,大多都属于有毒有害物质,会带来比较严重的环境问题。近年来,有人采用氧气替代传统的氧化剂来催化硫醇氧化制二硫醚,虽然无环境污染,但存在反应时间长、反应温度高、生产成本高等问题,并不适合大面积推广使用。
因此,有必要开发一种安全环保、条件温和、成本低的二硫醚制备方法。
发明内容
本发明的目的在于提供一种硫醇水相氧化制备二硫醚的方法。
本发明所采取的技术方案是:
一种硫醇水相氧化制备二硫醚的方法,包括以下步骤:有氧条件下,将催化剂加入硫醇水溶液中,20~100℃反应2~120min,得到二硫醚。
所述的硫醇为乙硫醇、丙硫醇、丁硫醇、戊硫醇、己硫醇、庚硫醇、辛硫醇、苯硫酚、2-甲基苯硫酚、3-甲基苯硫酚、4-甲基苯硫酚、4-甲氧基苯硫酚中的至少一种。
所述的硫醇水溶液的浓度为0.1wt%~60wt%。
所述的催化剂为负载型催化剂,活性组分为三氧化钨、五氧化二钒、三氧化钼、五氧化二铌、氧化铜、四氧化三钴、二氧化锰、三氧化二铁、二氧化铈、三氧化二镧中的至少一种,载体为活性炭、碳纳米纤维、碳纳米管中的至少一种。
所述的催化剂中活性组分所占的质量百分比为0.2%~40%。
所述的催化剂的添加量为硫醇水溶液质量的0.1%~50%。
本发明的有益效果是:本发明在水相中进行反应,以空气为氧化剂,无需使用有机溶剂,产物收率高,反应条件温和,反应过程绿色环保,生产成本低,适合大面积推广使用。
具体实施方式
一种硫醇水相氧化制备二硫醚的方法,包括以下步骤:有氧条件下,将催化剂加入硫醇水溶液中,20~100℃反应2~120min,得到二硫醚。
优选的,一种硫醇水相氧化制备二硫醚的方法,包括以下步骤:空气气氛下,将催化剂加入硫醇水溶液中,20~70℃反应10~80min,得到二硫醚。
优选的,所述的硫醇为乙硫醇、丙硫醇、丁硫醇、戊硫醇、己硫醇、庚硫醇、辛硫醇、苯硫酚、2-甲基苯硫酚、3-甲基苯硫酚、4-甲基苯硫酚、4-甲氧基苯硫酚中的至少一种。
优选的,所述的硫醇水溶液的浓度为0.1wt%~60wt%。
进一步优选的,所述的硫醇水溶液的浓度为0.2wt%~30wt%。
优选的,所述的催化剂为负载型催化剂,活性组分为三氧化钨、五氧化二钒、三氧化钼、五氧化二铌、氧化铜、四氧化三钴、二氧化锰、三氧化二铁、二氧化铈、三氧化二镧中的至少一种,载体为活性炭、碳纳米纤维、碳纳米管中的至少一种。
优选的,所述的活性炭为微孔碳(孔径小于2nm)、介孔炭(孔径2~50nm)、大孔碳(孔径大于50nm)中的至少一种。
优选的,所述的催化剂中活性组分所占的质量百分比为0.2%~40%。
进一步优选的,所述的催化剂中活性组分所占的质量百分比为0.5%~20%。
优选的,所述的催化剂的添加量为硫醇水溶液质量的0.1%~50%。
进一步优选的,所述的催化剂的添加量为硫醇水溶液质量的0.2%~30%。
优选的,所述的催化剂的制备方法包括以下步骤:先将活性组分配制成水溶液,再加入载体,混合均匀后静置10~15h,过滤,滤渣于100~120℃干燥10~15h,再在氮气气氛下300~800℃焙烧2~5h。
下面结合具体实施例对本发明作进一步的解释和说明。
编号1~12的催化剂中各组份的含量如下表所示:
表1编号1~12的催化剂的原料组成表
实施例1:丁硫醇的催化氧化反应
将10wt%的丁硫醇水溶液加入三口圆底烧瓶中,再加入催化剂(添加量为丁硫醇水溶液质量的10%),搅拌混合均匀,置于油浴中,加热至60℃,反应60min,反应结束后取样进行气相分析,测试结果如下表所示:
表2丁硫醇的催化氧化反应测试结果
催化剂编号 转化率(%) 二丁基二硫醚选择性(%)
1 90 >99
3 80 >99
6 92 >99
8 95 >99
10 93 >99
12 88 >99
实施例2:苯硫酚的催化氧化反应
将10wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂(添加量为苯硫酚水溶液质量的10%),搅拌混合均匀,置于油浴中,加热至60℃,反应60min,反应结束后,取样进行气相分析,测试结果如下表所示:
表3苯硫酚的催化氧化反应测试结果
实施例3:4-甲基苯硫酚的催化氧化反应
将10wt%的4-甲基苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂(添加量为4-甲基苯硫酚水溶液质量的10%),搅拌混合均匀,置于油浴中,加热至60℃,反应60min,反应结束后,取样进行气相分析,测试结果下表所示:
表4 4-甲基苯硫酚的催化氧化反应测试结果
催化剂编号 转化率(%) 对甲苯二硫醚选择性(%)
1 94 >99
4 92 >99
6 95 >99
7 100 >99
9 93 >99
12 90 >99
实施例4:反应温度对苯硫酚催化氧化反应的影响
将10wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂10(添加量为苯硫酚水溶液质量的10%),搅拌混合均匀,置于油浴中,加热至指定温度,反应60min,反应结束后,取样进行气相分析,测试结果如下表所示:
表5反应温度对苯硫酚催化氧化反应的影响
实施例5:
将30wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂10(添加量为苯硫酚水溶液质量的30%),搅拌混合均匀,置于油浴中,加热至60℃,反应80min,反应结束后,取样进行气相分析。
经测试,苯硫酚的转化率为92%,二苯二硫醚的选择性>99%。
实施例6:
将20wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂8(添加量为苯硫酚水溶液质量的10%),搅拌混合均匀,置于油浴中,加热至70℃,反应60min,反应结束后,取样进行气相分析。
经测试,苯硫酚的转化率为99%,二苯二硫醚的选择性>99%。
实施例7:
将5wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂5(添加量为苯硫酚水溶液质量的15%),搅拌混合均匀,置于油浴中,加热至30℃,反应70min,反应结束后,取样进行气相分析。
经测试,苯硫酚的转化率为80%,二苯二硫醚的选择性>99%。
实施例8:
将0.2wt%的苯硫酚水溶液加入三口圆底烧瓶中,再加入催化剂7(添加量为苯硫酚水溶液质量的0.2%),搅拌混合均匀,置于油浴中,加热至60℃,反应20min,反应结束后,取样进行气相分析。
经测试,苯硫酚的转化率为100%,二苯二硫醚的选择性>99%。
上述实施例为本发明较佳的实施方式,但本发明的实施方式并不受上述实施例的限制,其他的任何未背离本发明的精神实质与原理下所作的改变、修饰、替代、组合、简化,均应为等效的置换方式,都包含在本发明的保护范围之内。

Claims (1)

1.一种硫醇水相氧化制备二硫醚的方法,其特征在于:包括以下步骤:空气气氛下,将催化剂加入硫醇水溶液中,20~70℃反应10~80min,得到二硫醚;所述的催化剂为负载型催化剂,活性组分为三氧化钨、五氧化二钒、三氧化钼、五氧化二铌、氧化铜、四氧化三钴、二氧化锰、二氧化铈、三氧化二镧中的至少一种,载体为活性炭、碳纳米纤维、碳纳米管中的至少一种;所述的硫醇为乙硫醇、丙硫醇、丁硫醇、戊硫醇、己硫醇、庚硫醇、辛硫醇、苯硫酚、2-甲基苯硫酚、3-甲基苯硫酚、4-甲基苯硫酚、4-甲氧基苯硫酚中的至少一种;所述的硫醇水溶液的浓度为0.2wt%~30wt%;所述的催化剂中活性组分所占的质量百分比为0.5%~20%;所述的催化剂的添加量为硫醇水溶液质量的0.2%~30%。
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