Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzhydryl-3-(furan-2-ylmethoxy)-azetidine | HCID 67154603 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67154583 | HCID 67154583 | 74% |
Reaction Steps
1-Chloroethyl chloroformate (534 μL, 4.93 mmol) was added to a solution of 1-benzhydryl-3-(furan-2-ylmethoxy)-azetidine (1.5 g, 4.7 mmol) in dichloromethane (36 mL) at 0° C. The reaction mixture was then heated up to 40° C. and stirred for 2 hours. Ethanol (50 mL) was added and the reaction mixture was stirred for an additional 1 h30 at 40° C. After concentration to dryness, the crude mixture was triturated in petroleum ether (2×20 mL) to give a yellow oil (558 mg, 74%) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321769B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-b7f1ed11a8614a929d3b6ece0746fdc8 |
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| Source note | uspto-grants-2016_04 |
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