HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987515Generated: November 2, 2026
Ammonia → Dibenzyl 2-methylazetidine-1,2-dicarboxylate
https://huagongshe.com/reaction/1987515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | Dibenzyl azetidine-1,2-dicarboxylate | HCID 14683726 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dibenzyl 2-methylazetidine-1,2-dicarboxylate | HCID 66751005 | 77% |
Reaction Steps
A solution of Example 22A (325 mg, 1 mmol) and iodomethane (0.12 ml, 2.0 mmol) in THF (5 mL) was treated with NaN(TMS)2 in THF (1.0 M, 2 mL, 2.0 mmol) at −70° C. under nitrogen. The temperature of the cooling bath was slowly raised to −20° C. within 1 h and the mixture was stirred at the same temperature for additional 2 h. After quenching with water, the mixture was partitioned between water and EtOAc. The organic phase was washed with water and concentrated. The residue was purified on flash column chromatograph to give Example 22B. (250 mg, 77% yield). MS (DCI/NH3) m/z 340 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550603B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-65cbd183a9ca48a692b38bdafee78d0f |
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| Source note | uspto-grants-2009_06 |
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