Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 11759449 | HCID 11759449 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57420319 | HCID 57420319 | — |
Reaction Steps
A mixture of (3R,7aR)-7a-benzyl-3-trichloromethyl-tetrahydro-pyrrolo[1,2-c]oxazol-1one (1.40 g, prepared as described by Wang and Germanas Synlett 1999, 33-36.) and 7 M ammonia in MeOH (15 ml) was heated at 50° C. for 3 days in a sealed vessel. The cooled RM was then evaporated and triturated with chloroform to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357707B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-10cefa751531435ca46cfe99ee8b46da |
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| Source note | uspto-grants-2013_01 |
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