HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051839Generated: October 30, 2026
Diethyl Ether → 1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylate
https://huagongshe.com/reaction/1051839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 1-Boc-Azetidine-3-carboxylic acid | HCID 2755981 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-tert-Butyl 3-methyl azetidine-1,3-dicarboxylate | HCID 44607627 | — |
Reaction Steps
1-(t-butoxycarbonyl)azetidine-3-carboxylic acid (2.03 g, 10.09 mmol) was dissolved in MeOH (10 ml) and DCM (10 mL) and then cooled to 0° C. A 2M solution of trimethylsilyldiazomethane in ether (7.57 ml, 15.1 mmol) was then added drop-wise over 5 minutes. The solution was stirred for 10 minutes at 0° C. and then warmed to room temperature over 30 minutes. The solution was concentrated under reduced pressure to remove volatiles to afford crude 119, which was used directly in the next step without further purification. 1H NMR: 1.44 (s, 9H), 3.35 (m, 1H), 3.75 (s, 3H), 4.10 (d, 4H, J=7.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388191B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-fbe41c2954254c2482a399b489997861 |
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| Source note | uspto-grants-2016_07 |
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