preparation method of 1-chloro-4-(4-phenyl-1,3-butadiene)benzene_kain industrial additive

background and overview^[1]

1-chloro-4-(4-phenyl-1,3-butadiene)benzene can be used as a pharmaceutical synthesis intermediate.

preparation^[1]

1) synthesis of bisethyl-4-chlorobenzylphosphine

preparation process: preparation of bisethyl-4-chlorobenzylphosphine: 1-chloro-4-(chloromethyl)benzene (50g, 0.31mol) and triethyl phosphite (74.9g, 0.47mol) add to a 200 ml flask, heat to reflux and stir for 7 hours. the mixture is cooled to room temperature, and excess triethyl phosphite is distilled off under reduced pressure to obtain a crude product. the product in this step does not need to be purified and can be directly used in the next step of reaction.

2) synthesis of 41-chloro-4-(4-phenyl-1,3-butadiene)benzene

preparation process: add the product in 1 (39.4g, 0.15mol) to 100ml dry dmf, add 28% sodium methoxide (28.9g, 0.15mol) to the above solution, stir evenly, and add cinnamaldehyde (15.8g, 0.12mol)/dmf (10ml) solution was added to the mixture, and after stirring at room temperature for 10~15h, the mixture was poured into 300ml of water, and a small amount of hcl solution was added to obtain a large amount of white solid. filter and use 20ml of methanol. washes. then pour the white solid into 100ml methanol, stir, filter (twice), and dry under reduced pressure at 70°c to obtain white powder 1-chloro-4-(4-phenyl-1,3-butadiene)benzene , about 26g, yield 90%. (melting point, characterization data).

application

1-chloro-4-(4-phenyl-1,3-butadiene)benzene can be used as a pharmaceutical synthesis intermediate, if the following reaction occurs:

preparation process: accurately weigh 5.70g (0.02mol) of the product synthesized in the second step, 1-chloro-4-(4-phenyl-1,3-butadiene)benzene, in the glove box, 0.035g ( 0.1 mmol) 2-(dicyclohexylphosphino)biphenyl, 2.9 g (0.03 mol) sodium tert-butoxide and 0.022 g (0.1 mmol) palladium acetate. under ar gas protection, 1.49g (0.01mol) p-n-butylaniline and 150ml anhydrous and oxygen-free o-xylene were injected into the mixture, and the mixture was reacted at 130°c for 5 hours. after the reaction is completed, distill under reduced pressure at 80°c to obtain a brown liquid. cool to 15°c overnight to obtain a brown solid; after washing with o-xylene, dissolve the solid in o-xylene at 70°c. , add silica gel, stir for 2 hours, filter while hot, and wash the silica gel with o-xylene. collect the filtrate, distill under reduced pressure at 80°c, and cool to 15°c to obtain a yellow solid; filter, then wash with o-xylene, and finally use wash with ethyl acetate and dry under reduced pressure at 70°c to obtain yellow-green powder. yield 66%. characterization: m.p.160~161°c.1hnmr (400mhz, cdcl3): 7.42 (d, 4h, j=8hz), 7.29 (d, 8h, j=12hz), 7.21 (d, 2h, j=8hz), 7.08 (d, 2h, j=8hz), 7.02 (d, 6h, j=8hz), 6.97-6.91 (m, 2h), 6.87-6.81 (m, 2h), 6.62 (d, 2h, j=4hz), 6.60 (d, 2h, j=4hz), 2.58 (t, 2h, j=8hz), 1.64-1.56 (m, 2h), 1.42-1.33 (m, 2h), 0.94 (t, 3h, j=8hz) .

main reference materials

[1] (cn102516088) synthesis of a triphenylamine compound with strong fluorescence