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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426064Generated: October 31, 2026

3-Chloro-5-fluoro-2-methoxybenzaldehyde → HCID 58707255, compound

https://huagongshe.com/reaction/2426064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-5-fluoro-2-methoxybenzaldehydeHCID 13093560—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
ProductHCID 58707255HCID 5870725598%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-Fluoro-2-methoxy-3-chlorobenzaldehyde (2.0 g, 11.0 mmol) in dry diethyl ether (40 mL) at 0° C. was added methylmagnesium bromide of 3.0 M in ether (8.8 mL, 27.12 mmol). The reaction mixture was brought to room temperature and was stirred for 30 min then refluxed for 3 hours. 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-chlorophenyl)ethanol (2.1 g, 98%): 1H NMR (400 MHz, CDCl3): δ 7.12 (dd, 1H), 7.04 (dd, 1H), 5.19 (m, 1H), 3.84 (s, 3H), 2.18 (bs, 1H), 1.43 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968538B2
Source datasetuspto-grants-2011_06
ORD IDord-69309dc6c7694280adbf2b355e520cad
Source noteuspto-grants-2011_06