Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910622Generated: November 2, 2026

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

https://huagongshe.com/reaction/1910622

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 numberUS08604021B2
Source datasetuspto-grants-2013_12
ORD IDord-50c6d0149b6b4b58aaa8e8300e286b40
Source noteuspto-grants-2013_12