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Chemical Structure| 1007364-30-8 Chemical Structure| 1007364-30-8

Structure of 1007364-30-8

Chemical Structure| 1007364-30-8

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Product Details of [ 1007364-30-8 ]

CAS No. :1007364-30-8
Formula : C17H17NO4
M.W : 299.32
SMILES Code : O=C(O)/C(C1=CC=CC=C1COC2=CC=CC=C2C)=N/OC
MDL No. :MFCD30186605

Safety of [ 1007364-30-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H228-H315-H319
Precautionary Statements:P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:4.1
UN#:1325
Packing Group:

Application In Synthesis of [ 1007364-30-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1007364-30-8 ]

[ 1007364-30-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 143390-89-0 ]
  • [ 1007364-30-8 ]
YieldReaction ConditionsOperation in experiment
93.75% General procedure: (E,E)-2-[[1-(3-Trifluoromethylphenyl)ethylidene]aminooxymethyl]phenyl}-2-(methoxyimino)acetic acid (5) [7]. Sodium hydroxide (2.93 g, 0.073 mol) in water (120.0 mL) was added dropwise into a solution of Trifloxystrobin (1, 20.00 g, 0.049 mol) in toluene (200.0 mL) at 40-45 C. The bi-phasic reaction mixture was stirred at 65-70 C for 6.0 h. The reaction mixture was cooled to room temperature. Aqueous layer was separated, washed with toluene (50 mL), and then adjusted to pH 1.5 by adding concentrated hydrochloric acid at 10-15 C. The white slurry obtained was extracted in ethyl acetate (50 mL 2).The ethyl acetate extracts were combined, washed with water (50 mL 2), dried over anhydrous sodium sulfate and then concentrated to yield acid 5 (white solid, 18.5 g,0.047 mol, 95.92%);
92% With water; sodium hydroxide; In methanol; for 3h;Reflux; In a 250 mL round bottom flask, 7.58 g (24.2 mmol) of P1 was added. 100 mL of methanol and 24.2 ml of aqueous sodium hydroxide solution (3 mol/L), the mixture was heated to reflux for 3 h, and then the reaction was taken to the reaction by TLC. The reaction solution was spun and poured into dichloromethane. Wash with 3% dilute hydrochloric acid solution until neutral, extract three times with dichloromethane. The extract was washed three times with saturated saline solution, Dry over anhydrous magnesium sulfate, filter, and evaporate on a rotary evaporator. Recrystallization, giving 7.01 g of a final white solid. The yield was 92%.
 

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