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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602824Generated: October 31, 2026

Trimethyl orthoformate → HCID 57948569, compound

https://huagongshe.com/reaction/602824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium HydroxideHCID 14798—
Reactant3-azetidinecarboxylic AcidHCID 93192—
ReactantSodium borohydrideHCID 4311764—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 86635605HCID 86635605—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57948569HCID 5794856962.7%

Reaction Steps

Azetidine-3-carboxylic acid (46 mg) and sodium hydroxide (18 mg) were dissolved in methanol (4 mL). To this solution, trimethoxymethane (0.050 mL) and a tetrahydrofuran (1 mL)-methanol (1 mL) mixed solution of 6-[3-(4-chlorophenyl)propoxy]-3,4-dihydronaphthalene-2-carboaldehyde (100 mg) were successively added under ice cooling. The reaction mixture was stirred for 3.5 hours under ice cooling. To the reaction mixture, sodium borohydride (17 mg) was added under ice cooling. The reaction mixture was stirred under ice cooling for 20 minutes. Thereafter, 4 mol/L hydrogen chloride/ethyl acetate solution was added until it was neutral, and concentrated. The obtained residue was purified by flash silica gel column chromatography (chloroform:methanol:aqueous ammonia=80:10:1 to 80:20:4), to thereby obtain the title compound (79 mg) having the following physical properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906549B2
Source datasetuspto-grants-2011_03
ORD IDord-288b3d231a7c42c6ad0d3e8a46d329fb
Source noteuspto-grants-2011_03