HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627561Generated: November 1, 2026
Trimethylsilyldiazomethane → 1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylate
https://huagongshe.com/reaction/1627561
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 | US08785632B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-2166c18b1ac64904a4af15db40458c14 |
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| Source note | uspto-grants-2014_07 |
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