Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 70664654 | HCID 70664654 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 70664502 | HCID 70664502 | — |
Reaction Steps
cis-2-Benzyl-6-(difluoromethyl)-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole (0.070 mmol, 23 mg) was dissolved in toluene (1 ml) and ACE-Cl (0.492 mmol, 0.054 ml, 70.3 mg) was added. The reaction mixture was heated to 160° C. for 15 minutes in a microwave reactor. MeOH (1 ml) was added and the reaction mixture was heated for a further 5 minutes at 160° C. in a microwave reactor and then the resulting solution was passed through an SCX cartridge. The fractions containing the desired product were concentrated in vacuo and then purified by silica column chromatography (eluting with DCM then 2-16% MeOH(NH3) in DCM) to give a crude residue that was dissolved in DCM and 2N HCl in ether (1 ml) was added. The solvent was removed in vacuo to afford cis-6-(difluoromethyl)3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole hydrochloride (13 mg), m/z: 238.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729274B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-576bedb179674f54899d652d6e2b1a75 |
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| Source note | uspto-grants-2014_05 |
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