Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 67154610 | HCID 67154610 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67154616 | HCID 67154616 | 77% |
Reaction Steps
1-Chloroethyl chloroformate (218 μL, 2.0 mmol) was added to a solution of 1-benzhydryl-3-((4-bromothiophen-2-yl)methoxy)-azetidine (793 mg, 1.91 mmol) in dichloromethane (10 mL). The reaction mixture was stirred for 1 hour at 0° C. and for an additional 1 hour at room temperature. Ethanol (10 mL) was then added and the reaction mixture was stirred overnight. After concentration to dryness, the crude mixture was precipitated from a mixture dichloromethane/diethyl ether to afford a white solid (417 mg, 77%) which was used in the next step whitout further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846711B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ee83126c36254b20be8224bd85b42705 |
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| Source note | uspto-grants-2014_09 |
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