Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 67154550 | HCID 67154550 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 67154642 | HCID 67154642 | 90% |
Reaction Steps
1-Chloroethyl chloroformate (180 μL, 1.6 mmol) was added to a solution of 1-benzhydryl-3-butoxyazetidine (370 mg, 1.2 mmol) in 1,2-dichloroethane (6 mL) at room temperature. The reaction mixture was then heated up to 70° C. and stirred for 1.5 hours. After cooling down to room temperature, methanol (7 mL) was added. The reaction mixture was again heated up to 70° C. and stirred for an additional 1.5 hours. After concentration to dryness, the crude mixture was triturated in pentane (2×5 mL) to give a yellow oil (179 mg, 86%) 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 | US08846711B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-95f30f31f97f486aa7cdaaeb3b3284b4 |
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| Source note | uspto-grants-2014_09 |
|---|