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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528751Generated: October 28, 2026

Water → tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/528751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylateHCID 10583745—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-(methoxymethyl)azetidine-1-carboxylateHCID 66570673—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 24.6 mg (0.74 mmol, 60% dispersion in mineral oil) NaH in 5 mL THF at 0° C. was added 0.115 g (0.61 mmol) 3-hydroxymethyl-azetidine-1-carboxylic acid tert-butyl ester (prepared using route 15 step a) in 1 mL THF dropwise over 10 minutes, and the reaction was stirred at 0° C. for 30 minutes. 46 μL (0.74 mmol) methyl iodide was added and the reaction was stirred at room temperature for 2 hours. 20 mg (0.61 mmol, 60% dispersion in mineral oil) of NaH followed by 38 μL (0.61 mmol) of methyl iodide were added and the reaction mixture was stirred at room temperature for 16 hours. 5 mL of H2O was added and the mixture was extracted with EtOAc (2×10 mL), the organic layers were combined and dried with MgSO4. After filtration, the solvent was evaporated to give the desired product which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-109e65e411d246dab2ed8ef7bb547e7b
Source noteuspto-grants-2016_05