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ChemicalBook CAS DataBase List 2,4-Dichlorophenylacetonitrile
6306-60-1

2,4-Dichlorophenylacetonitrile synthesis

10synthesis methods
sodium:cyanide

773837-37-9

2,4-Dichlorobenzyl chloride

94-99-5

2,4-Dichlorophenylacetonitrile

6306-60-1

General method: 2,4-dichlorobenzyl chloride (1.0 mmol) was mixed with sodium cyanide (2 mmol) in deionized water (5 mL) and polyethylene glycol modified diisocyanate (PEG-MDIL, 0.2 g) was added. The reaction suspension was placed under reflux conditions and the reaction mixture was stirred using a magnetic stirrer for the reaction time referred to in Table 2.After completion of the reaction, the mixture was extracted with ether (2 × 10 mL). The organic extracts were combined, dried with anhydrous calcium chloride and subsequently concentrated under reduced pressure. By this method, the target product 2,4-dichlorophenylacetonitrile was obtained in good to excellent isolated yields (see Scheme 3).

773837-37-9 Synthesis
sodium:cyanide

773837-37-9
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Yield:6306-60-1 93%

Reaction Conditions:

in ethanol;water

Steps:

8 Example 8
To a 100 mL round bottom flask was added 2,4-dichlorobenzyl bromide(24 g, 0.1 mol) and ethanol (30 mL) and water (5 mL)Subsequently, sodium cyanide (4.9 g, 0.1 mol) was added and the reaction was stirred. After completion of the reaction, the resulting organic phase was separated and distilled to give 17.30 g of 2,4-dichlorophenylacetonitrile in 93% yield.

References:

Zhejiang Yongtai Pharmaceutical Co., Ltd.;Jin Yizhong;He Renbao;Zhou Guobin;Xie Jianren CN106117028, 2016, A Location in patent:Paragraph 0059; 0060

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