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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544332Generated: November 2, 2026

Methanol → 2-Chloro-6-methoxybenzaldehyde

https://huagongshe.com/reaction/544332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-6-fluorobenzaldehydeHCID 67847—
Product2-Chloro-6-methoxybenzaldehydeHCID 1096497164.2%

Reaction Steps

2-Chloro-6-fluorobenzaldehyde (51.5 g., 0.030 mole) was taken into 500 ml. of methanol. Sodium hydroxide (14.4 g., 0.35 mole) was added and the stirred reaction mixture heated to reflux for 3 hours. The mixture was cooled to room temperature, and the volume reduced to 200 ml. by distillation in vacuo. Water (400 ml.) and methylene chloride (200 ml.) were added and the two phase system equilibrated. The organic phase was separated and the aqueous phase extracted with two additional 100 ml. portions of methylene chloride. The combined organic layers were dried over anhydrous sodium sulfate, filtered and the methylene chloride removed by distillation at atmospheric pressure with displacement by hexane (450 ml.) to a final volume of 300 ml. The product layer, initially present as an oil, began to crystallize at 45° C. The mixture was cooled to room temperature, granulated for 16 hours, and filtered to yield 2-chloro-6-methoxybenzaldehyde [35.6 g., 64.2%; Rf 0.2 (CHCl3 )].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448971
Source datasetuspto-grants-1984_05
ORD IDord-c5ce4c3898b747b1affb54aa64e412b5
Source noteuspto-grants-1984_05