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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266697Generated: October 30, 2026

Trimethylsilyldiazomethane → 1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylate

https://huagongshe.com/reaction/2266697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylateHCID 44607627—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(t-butoxycarbonyl) azetidine-3-carboxylic acid (1-1)(AXL016917, 1000 mg, 4.97 mmol) was dissolved in MeOH (5 mL)/Toluene (20 mL) and then cooled to 0° C. TMSCHNN (trimethylsilyldiazomethane) (7.45 mmol) was then added drop-wise over 15 minutes with some bubbling observed. The color started clear and slowly turned yellow. The solution was stirred for 10 minutes at 0° C. and then warmed to room temperature over 30 minutes. The solution was then concentrated and pumped on to remove toluene to afford 1.055 g of 1-t-butyl 3-methyl azetidine-1,3-dicarboxylate (1-2) that was used directly in the next step without being purified (99% crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858643B2
Source datasetuspto-grants-2010_12
ORD IDord-7202f5d819f843d1a2bf4bfa870e2f67
Source noteuspto-grants-2010_12