RU2012141443A - METHOD FOR PRODUCING 5-METHOXICARBONIL-1,3-DITIAN, FUNGICIDAL ACTIVITY - Google Patents

METHOD FOR PRODUCING 5-METHOXICARBONIL-1,3-DITIAN, FUNGICIDAL ACTIVITY Download PDF

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RU2012141443A
RU2012141443A RU2012141443/04A RU2012141443A RU2012141443A RU 2012141443 A RU2012141443 A RU 2012141443A RU 2012141443/04 A RU2012141443/04 A RU 2012141443/04A RU 2012141443 A RU2012141443 A RU 2012141443A RU 2012141443 A RU2012141443 A RU 2012141443A
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dithian
cocl
methoxycarbonyl
fungicidal activity
hydrogen sulfide
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RU2012141443/04A
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RU2536205C2 (en
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Усеин Меметович Джемилев
Внира Рахимовна Ахметова
Наиль Салаватович Ахмадиев
Екатерина Владимировна Федорова
Любовь Федоровна Коржова
Наиля Фауатовна Галимзянова
Асхат Габдрахманович Ибрагимов
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Федеральное Государственное Бюджетное Учреждение Науки Институт Нефтехимии И Катализа Ран
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Abstract

1. Способ получения 5-метоксикарбонил-1,3-дитиана общей формулы (1), обладающего фунгицидной активностью,отличающийся тем, что насыщенный сероводородом водный раствор формальдегида (37%) подвергают взаимодействию с диметиловым эфиром малоновой кислоты в присутствии катализатора CoClпри мольном соотношении формальдегид: сероводород: диметиловый эфир малоновой кислоты: CoCl, равном 3:2:1: (0,03-0,07), при комнатной температуре (~20°С) и атмосферном давлении в течение 4-6 ч.2. Применение 5-метоксикарбонил-1,3-дитиана в качестве фунгицида по отношению к Bipolaris sorokiniana.1. A method of obtaining 5-methoxycarbonyl-1,3-dithian of the general formula (1) having fungicidal activity, characterized in that the aqueous solution of formaldehyde saturated with hydrogen sulfide (37%) is reacted with malonic acid dimethyl ether in the presence of a CoCl catalyst in a molar ratio of formaldehyde : hydrogen sulfide: malonic acid dimethyl ether: CoCl, equal to 3: 2: 1: (0.03-0.07), at room temperature (~ 20 ° C) and atmospheric pressure for 4-6 hours. 2. The use of 5-methoxycarbonyl-1,3-dithian as a fungicide with respect to Bipolaris sorokiniana.

Claims (2)

1. Способ получения 5-метоксикарбонил-1,3-дитиана общей формулы (1), обладающего фунгицидной активностью,1. The method of obtaining 5-methoxycarbonyl-1,3-dithian of General formula (1) having fungicidal activity,
Figure 00000001
Figure 00000001
отличающийся тем, что насыщенный сероводородом водный раствор формальдегида (37%) подвергают взаимодействию с диметиловым эфиром малоновой кислоты в присутствии катализатора CoCl2 при мольном соотношении формальдегид: сероводород: диметиловый эфир малоновой кислоты: CoCl2, равном 3:2:1: (0,03-0,07), при комнатной температуре (~20°С) и атмосферном давлении в течение 4-6 ч.characterized in that the aqueous solution of formaldehyde saturated with hydrogen sulfide (37%) is reacted with malonic acid dimethyl ether in the presence of a CoCl 2 catalyst at a molar ratio of formaldehyde: hydrogen sulfide: malonic acid dimethyl ether: CoCl 2 equal to 3: 2: 1: (0, 03-0.07), at room temperature (~ 20 ° C) and atmospheric pressure for 4-6 hours
2. Применение 5-метоксикарбонил-1,3-дитиана в качестве фунгицида по отношению к Bipolaris sorokiniana. 2. The use of 5-methoxycarbonyl-1,3-dithian as a fungicide with respect to Bipolaris sorokiniana.
RU2012141443/04A 2012-09-27 2012-09-27 Method of obtaining 5-methoxycarbonyl-1,3-dithiane, possessing fungicidal activity RU2536205C2 (en)

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SU586174A1 (en) * 1976-04-26 1977-12-30 Уфимский Нефтяной Институт Method of preparing 1,3-dithiacycloalkanes
GB9027571D0 (en) * 1990-12-19 1991-02-06 Wellcome Found Novel heterocyclic pesticidal compounds
WO2000040576A2 (en) * 1999-01-07 2000-07-13 Fujisawa Pharmaceutical Co., Ltd. Thiopyran compounds as inhibitors of mmp

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