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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298723Generated: October 31, 2026

2-Bromo-5-methoxybenzaldehyde → HCID 18377949, compound

https://huagongshe.com/reaction/2298723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-methoxybenzaldehydeHCID 344480—
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
ProductHCID 18377949HCID 18377949—

Reaction Steps

Similarly to the method described by Kumar, S., J.Org.Chem. 62, 8535 (1997), 2-bromo-5-methoxy-benzaldehyde (for preparation see Ex. 1) and 4-trifluoromethoxyphenylboronic acid {prepared in a conventional manner from 4-trifluoromethoxy-bromobenzene [407-14-7]} are reacted to give 2-formyl-4-propyloxy-4′-trifluoromethoxy-biphenyl. Similarly to the method described in the same reference, this compound is reacted with trimethylsulfonium iodide under phase transfer conditions to give the corresponding oxiranyl derivative which can be isolated, but can alternatively advantageously be directly converted into the target compound by reaction with methanesulfonic acid (as described by Kumar, loc. cit.). Aqueous workup can be followed by purification as described in Ex. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495220B2
Source datasetuspto-grants-2002_12
ORD IDord-dd7cb7a3bbe749a08c44a217d5fd5d57
Source noteuspto-grants-2002_12