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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910580Generated: October 25, 2026

5-Chloro-2,3-dimethoxybenzaldehyde → 1-(5-Chloro-2,3-dimethoxyphenyl)ethanol

https://huagongshe.com/reaction/1910580

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2,3-dimethoxybenzaldehydeHCID 4172275—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-(5-Chloro-2,3-dimethoxyphenyl)ethanolHCID 1409291575%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-chloro-2,3-dimethoxy-benzaldehyde (7.0 g, 34.90 mmol) in dry diethyl ether (500 mL) at 0° C. was added methylmagnesium bromide of 3.0 M in diethyl ether (29 mL, 87.22 mmol). The reaction mixture was brought to room temperature and stirred for 30 min; refluxed for 3 h; then cooled to 0° C. and quenched by adding saturated aqueous NH4Cl. The two liquid layers were separated. The aqueous layer was extracted with diethyl 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-chloro-2,3-dimethoxy-phenyl)-ethanol (5.67 g, 75%): 1H NMR (400 MHz, CDCl3): δ 7.00 (d, 1 H), 6.81 (d, 1 H), 5.11 (m, 1 H), 3.86 (s, 6 H), 2.30 (d, 1 H), 1.48 (d, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604021B2
Source datasetuspto-grants-2013_12
ORD IDord-ecdf62a3bd264499b0564affada312f0
Source noteuspto-grants-2013_12