Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 13060145 | HCID 13060145 | — |
| Reactant | HCID 23359463 | HCID 23359463 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 57097879 | HCID 57097879 | — |
Reaction Steps
To a suspension of the title compound of Step E above (2.2 g, 0.005 mol) in25 ml methylene chloride cooled to 0° C. was added triethylamine (1.0 g) and hexyl (chlorosulfenyl)(methyl)carbamate, (prepared in a mannersimilar to Example 1, Step D), (2.5 g 75% pure) dropwise at 0° C. The mixture was stirred at room temperature for additional one hour. The reaction mixture was concentrated under high vacuum and subjected to silica gel column chromatography using hexane-ether (1:1) as an eluent. The title compound (2.5 g) was obtained, melting point 128°-129° C. in high purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491162 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-1f47a50b14f443b3bdc16b53660ed257 |
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| Source note | uspto-grants-1996_02 |
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