HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170944Generated: October 30, 2026
Isopropanol → 4-Bromo-2-(trifluoromethoxy)benzaldehyde
https://huagongshe.com/reaction/2170944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | 4-Bromo-2-(trifluoromethoxy)iodobenzene | HCID 2736422 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Bromo-2-(trifluoromethoxy)benzaldehyde | HCID 18700087 | — |
Reaction Steps
20.00 g (54.51 mmol) of 4-bromo-2-(trifluoromethoxy)iodobenzene are dissolved in 200 ml of THF and cooled to −78° C. Then 26.16 ml (65.41 mmol) of a 2.5 M solution of n-butyllithium in hexane are added dropwise. The mixture is stirred for 30 min and then 14.43 g (125.37 mmol) of N-formylmorpholine are metered in. After complete conversion is detected (TLC check), solvolysis is carried out at −78° C. with isopropanol. Warming to room temperature is followed by addition of water and extraction twice with dichloromethane. The combined organic phases are washed with saturated sodium chloride solution and dried with sodium sulfate, and the solvent is distilled out under reduced pressure. The residue is purified by column chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate 5:1). 11.43 g (78% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051316B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d005ac4e7bf548bc8a15c6d08e9f513d |
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| Source note | uspto-grants-2015_06 |
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