Monoterpene phenolic derivative, synthetic method of monoterpene phenolic derivative and application of monoterpene phenolic derivative in pesticides
A synthesis method and monoterpene phenol technology are applied in the field of pesticides and achieve the effects of good bactericidal effect, simple structure and easy synthesis.
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[0033] Its synthetic steps of the synthetic method of monoterpene phenol compound of the present invention are as follows:
[0034]
[0035] The application of the monoterpene phenolic compound of the present invention in pesticides is used to inhibit or kill phytopathogenic fungi, and the phytopathogenic fungi that are inhibited or killed are tomato early blight, tomato cinerea, cucumber fusarium wilt, and rice blast fungus or rice sheath blight.
Embodiment 1
[0036] Embodiment 1: monoterpene phenolic compound (C 12 h 15 ClO 2 )Synthesis.
[0037] The concrete steps of the synthetic method of this monoterpene phenol compound are as follows:
[0038] (1) Synthesis of intermediate 5-methyl-2-isopropyl-4-chlorophenol
[0039] 1.5 g of thymol was dissolved in 20 mL of dichloromethane, and the resulting solution was cooled to 0°C. A solution of 1.6 g of sulfonyl chloride in dichloromethane (5 mL) was slowly added within 20 min using a constant pressure dropping funnel, and the resulting mixture was continued to react at room temperature after the addition was complete. TLC monitors the progress of the reaction. After the reaction is completed, add 30 mL of distilled water, extract three times with 30 mL of ethyl acetate, combine the organic phases, dry and concentrate, and use eluent (petroleum ether: ethyl acetate=50:1) column chromatography to obtain the compound 5-Methyl-2-isopropyl-4-chlorophenol, yield 78%, pale yellow oil. ...
Embodiment 2
[0050] Embodiment 2: monoterpene phenolic compound (C 12 h 15 BrO 2 )Synthesis.
[0051] The concrete steps of the synthetic method of this monoterpene phenol compound are as follows:
[0052] (1) Synthesis of intermediate 5-methyl-2-isopropyl-4-bromophenol
[0053] 1.218 g of thymol was dissolved in 20 mL of acetic acid, and the resulting solution was cooled to 0°C. Add 0.51 mL of Br slowly within 20 min using a constant pressure dropping funnel 2 , After the dropwise addition was completed, the resulting mixture was stirred at room temperature for 6 h. The reaction was poured into 50 mL of ice water, extracted three times with 30 mL of dichloromethane, the organic phases were combined, dried and concentrated, and the intermediate 5-methanol was obtained by column chromatography with eluent (petroleum ether: ethyl acetate=40:1). 2-isopropyl-4-bromophenol, yield 82%, pale yellow oil.
[0054] (2) Synthesis of the target compound
[0055] Take 229mg of the intermediat...
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