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General procedure: mmol), ethyl chloroacetate (0.147 g, 2.4 mmol), K2CO3(0.28 g,4 mmol) and DMF(10 ml) was stirred at 6 C for 12 h. DMF wasremoved under reduced pressure and the residue was purifiedthrough a column chromatography on silica with chloroform/methanol (V:V 50:1) as a white solid (0.59 g, 95.2% yield).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 1-(3-Chloropropyl)-1H-imidazole, other downstream synthetic routes, hurry up and to see.

Reference:
Article; Fan, Yan-Hua; Li, Wei; Liu, Dan-Dan; Bai, Meng-Xuan; Song, Hong-Rui; Xu, Yong-Nan; Lee, SangKook; Zhou, Zhi-Peng; Wang, Jian; Ding, Huai-Wei; European Journal of Medicinal Chemistry; vol. 139; (2017); p. 95 – 106;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem