HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396308Generated: November 1, 2026
5-Chloro-2-(difluoromethoxy)benzaldehyd → HCID 86721086, compound
https://huagongshe.com/reaction/1396308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Chloro-2-(difluoromethoxy)benzaldehyd | HCID 4770949 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86721086 | HCID 86721086 | 103% |
Reaction Steps
5-Chloro-2-(difluoromethoxy)benzaldehyde (0.480 g, 2.324 mmol) was dissolved in dry THF (11.62 mL) and the reaction was cooled to −78° C. under argon. Vinyl magnesium bromide (3.49 mL, 3.49 mmol) was then added dropwise. After the reaction was complete, the ice bath was removed and reaction was allowed to warm to rt and stirred for an additional 2 h. The reaction was cooled to 0° C. and then carefully quenched with saturated ammonium chloride. The mixture was then diluted with water and extracted with EtOAc (3×). The combined organic phases were dried over Na2SO4, filtered and concentrated to yield 1-(5-chloro-2-(difluoromethoxy)phenyl)prop-2-en-1-ol (561 mg, 103%) as a clear oil. MS (ESI) m/z: 236.9 (M+H, Chlorine isotope peak)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901115B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-3ad229c87ba9493ca16a142808fb960a |
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| Source note | uspto-grants-2014_12 |
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