二硫代乙酸乙酯

二硫代乙酸乙酯
识别
CAS号	870-73-5
PubChem	70093
性质
化学式	C4H8S2
摩尔质量	120.24 g·mol−1
外观	黄色液体[1]
沸点	61 °C（23 mmHg）[1]
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

二硫代乙酸乙酯是一种有机化合物，化学式为C₄H₈S₂。它可以乙腈、乙硫醇和盐酸为原料反应，经碳酸钾处理后再与硫化氢反应制得；[1]或由2,4-二乙硫基-1,3,2,4-二硫杂二磷杂环丁烷-2,4-二硫化物和乙酸反应得到。[2]它和双(三氟甲基)二甲氨基硼反应，可以得到双(三氟甲基)(二甲胺)硼基二硫代乙酸乙酯。[3]

参考文献

Marvel, C. S.; de Radzitzky, P.; Brader, James J. . Journal of the American Chemical Society (American Chemical Society (ACS)). 1955, 77 (22): 5997–5999. ISSN 0002-7863. doi:10.1021/ja01627a060.
Davy, Hubert. . Journal of the Chemical Society, Chemical Communications (Royal Society of Chemistry (RSC)). 1982, (8): 457. ISSN 0022-4936. doi:10.1039/c39820000457.
Buerger, H.; Pawelke, G.; Rothe, J. Ene-type and hydride-shift reactions of thiocarbonyl compounds with (dimethylamino)bis(trifluoromethyl)borane, (CF3)2BNMe2. Journal of Organometallic Chemistry, 1994. 474 (1-2): 43-48. ISSN 0022-328X.

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[ref-1] Marvel, C. S.; de Radzitzky, P.; Brader, James J. . Journal of the American Chemical Society (American Chemical Society (ACS)). 1955, 77 (22): 5997–5999. ISSN 0002-7863. doi:10.1021/ja01627a060.

[2] Davy, Hubert. . Journal of the Chemical Society, Chemical Communications (Royal Society of Chemistry (RSC)). 1982, (8): 457. ISSN 0022-4936. doi:10.1039/c39820000457.

[3] Buerger, H.; Pawelke, G.; Rothe, J. Ene-type and hydride-shift reactions of thiocarbonyl compounds with (dimethylamino)bis(trifluoromethyl)borane, (CF3)2BNMe2. Journal of Organometallic Chemistry, 1994. 474 (1-2): 43-48. ISSN 0022-328X.