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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 1-Boc-Azetidine-3-carboxylic acid | HCID 2755981 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylate | HCID 44607627 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858643B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-7202f5d819f843d1a2bf4bfa870e2f67 |
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| Source note | uspto-grants-2010_12 |
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