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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216534Generated: November 1, 2026

2-(Bromomethyl)-4'-chloro-4-methoxy-1,1'-biphenyl → Methyl (2E)-3-(2-{4-[(4'-chloro-4-methoxy-1,1'-biphenyl-2-yl)methoxy]phenyl}-1-cyclohexyl-1H-imidazol-4-yl)-2-propenoate

https://huagongshe.com/reaction/2216534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)-4'-chloro-4-methoxy-1,1'-biphenylHCID 21943338—
ReactantMethyl (2E)-3-{2-[4-(hydroxy)phenyl]-1-cyclohexyl-1H-imidazol-4-yl}-2-methyl-2-propenoateHCID 136341818—
ProductMethyl (2E)-3-(2-{4-[(4'-chloro-4-methoxy-1,1'-biphenyl-2-yl)methoxy]phenyl}-1-cyclohexyl-1H-imidazol-4-yl)-2-propenoateHCID 1134193773.2%

Reaction Steps

According to the procedure for preparation of 4.4, phenol 12.9 (60 mg, 0.184 mmol) was alkylated with (4′-chloro-4-methoxy-1,1′-biphenyl-2-yl)methyl bromide (63 mg, 0.202 mmol), to yield 75 mg (73%) of 12.10. MS (ESI) 557.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112601B2
Source datasetuspto-grants-2006_09
ORD IDord-ee5eae4a1b084888b1ba8fc351c0edeb
Source noteuspto-grants-2006_09