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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481296Generated: October 25, 2026

3-Chloro-2,6-difluorobenzaldehyde → 1-(3-Chloro-2,6-difluorophenyl)-2-methylprop-2-en-1-ol

https://huagongshe.com/reaction/1481296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2,6-difluorobenzaldehydeHCID 736338—
ReactantHCID 178456138HCID 178456138—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Chloro-2,6-difluorophenyl)-2-methylprop-2-en-1-olHCID 11823606552%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of prop-1-en-2-ylmagnesium bromide (0.5M in THF) (2 mL, 1.000 mmol) was added 3-chloro-2,6-difluorobenzaldehyde (136 mg, 0.769 mmol) in THF (1 mL) dropwise at 0° C. under Ar and stirred at 0° C. for 15 mins. The reaction mixture was quenched with sat. aq.NH4Cl and extracted with ether. The organic phase was washed with sat. aq.NH4Cl and brine, dried over MgSO4, filtered, and concentrated. Purification by flash chromatography to yield 73A as colorless oil (87 mg, 52%). 1H NMR (400 MHz, CHLOROFORM-d) δ 7.36-7.28 (m, 1H), 6.91-6.83 (m, 1H), 5.48 (d, J=9.2 Hz, 1H), 5.12-5.06 (m, 1H), 5.04-4.99 (m, 1H), 2.56 (dt, J=9.2, 2.2 Hz, 1H), 1.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409908B2
Source datasetuspto-grants-2016_08
ORD IDord-46e77794eac649339a554e6295ca6f66
Source noteuspto-grants-2016_08