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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-5-methoxybenzaldehyde | HCID 344480 | — |
| Reactant | 1-Bromo-4-(trifluoromethoxy)benzene | HCID 521008 | — |
| Reactant | 4-(Trifluoromethoxy)phenylboronic acid | HCID 2734386 | — |
| Product | HCID 18377949 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495220B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-dd7cb7a3bbe749a08c44a217d5fd5d57 |
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| Source note | uspto-grants-2002_12 |
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