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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956567Generated: October 31, 2026

Water → 2-Chloro-6-phenoxybenzenemethanol

https://huagongshe.com/reaction/1956567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-chloro-6-phenoxybenzaldehydeHCID 18663602—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-6-phenoxybenzenemethanolHCID 2237837694%

Reaction Steps

19.0 g (77.67 mmol) of 2-chloro-6-phenoxybenzaldehyde in approximately 40 ml of tetrahydrofuran are added dropwise at room temperature in the course of 30 minutes to a suspension of 4.42 g (116.5 mmol) of lithium aluminium hydride in approximately 150 ml of tetrahydrofuran. The mixture is then heated under reflux for 4 hours, cooled and hydrolysed with 4.4 ml of water, 4.4 ml of 4N sodium hydroxide and 13.2 ml of water. The reaction mixture is boiled under reflux for 30 minutes, cooled and filtered, and the suction filter residue is 3× taken up in ethyl acetate, boiled under reflux for 15 minutes and filtered. The combined filtrates are concentrated. 17.97 g (76.57 mmol)=94% of crude (2-chloro-6-phenoxy-phenyl)-methanol are obtained in the form of a yellow oil; TLC (silica gel; ethyl acetate/hexane=1:1; UV): Rf =0.68; 1H-NMR (CDCl3, 200 MHz): 4.90 (s, 2H); 6.76-7.40 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780500
Source datasetuspto-grants-1998_07
ORD IDord-d332945993db4d0b81ad63a03c8afc08
Source noteuspto-grants-1998_07