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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910628Generated: November 3, 2026

5-Fluoro-2-methoxy-3-methylbenzaldehyde → HCID 58707309, compound

https://huagongshe.com/reaction/1910628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methoxy-3-methylbenzaldehydeHCID 58707319—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
ProductHCID 58707309HCID 5870730976%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-Fluoro-2-methoxy-3-methylbenzaldehyde (1.2 g, 7.13 mmol) in dry diethyl ether (20 mL) at 0° C. was added methylmagnesium bromide of 3.0 M in ether (6.0 mL, 17.83 mmol). The reaction mixture was brought to room temperature and was stirred for 30 min. then refluxed for 3 h. It was then cooled to 0° C. and quenched by adding saturated aqueous NH4Cl. The two liquid layers were separated. The aqueous layer was extracted with ether. The combined organic layers were washed with water, dried, and concentrated to the crude compound which was purified by silica gel column (10-25% ethyl acetate in hexanes) to afford 1-(5-fluoro-2-methoxy-3-methylphenyl)ethanol (1.0 g, 76%): 1H NMR (400 MHz, CDCl3): δ 7.12 (dd, 1H), 6.83 (dd, 1H), 4.72 (m, 1H), 3.81 (s, 3H), 2.38 (s, 3H), 1.47 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604021B2
Source datasetuspto-grants-2013_12
ORD IDord-77b91383e8ce4e978e61980aaa101481
Source noteuspto-grants-2013_12