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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-(difluoromethoxy)benzaldehydHCID 4770949—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86721086HCID 86721086103%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901115B2
Source datasetuspto-grants-2014_12
ORD IDord-3ad229c87ba9493ca16a142808fb960a
Source noteuspto-grants-2014_12