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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322978Generated: October 30, 2026

Sodium hydride → 2-Methyl-5-(2-(trimethylsilyl)ethoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/322978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Hydroxy-2-methylbenzaldehydeHCID 585875—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Product2-Methyl-5-(2-(trimethylsilyl)ethoxymethoxy)benzaldehydeHCID 22010444103.3%

Reaction Steps

5-hydroxy-2-methylbenzaldehyde (3.4 g) is added portionwise to a stirred suspension of sodium hydride (1.2 g, 60% dispersion in mineral oil). The reaction mixture is stirred at room temperature for 45 minutes, 2-(trimethylsilyl)ethoxymethyl chloride (5 g) is added slowly and stirring continued for a further 3 hours. The mixture is evaporated and the residue partitioned between ethyl acetate (50 mL) and water (150 mL). The organic phase is washed with brine (150 mL) dried over magnesium sulphate and evaporated to give 2-methyl-5-(2-(trimethylsilyl)ethoxymethoxy)benzaldehyde (6.87 g) as a red-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211234B1
Source datasetuspto-grants-2001_04
ORD IDord-bef07d2b69304082860c6aab2ee987ee
Source noteuspto-grants-2001_04