Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (Cyclopentylsulfanyl)acetic acid | HCID 15728315 | — |
| Product | HCID 86665181 | HCID 86665181 | — |
Reaction Steps
The product from Example 143B (6.56 g) was combined with thionyl chloride (50 mL, 685 mmol) and the reaction mixture was heated at 70° C. for 2 hours. The reaction mixture was concentrated under vacuum, and the residue was dissolved in CHCl3 (50 mL) and concentrated again to remove excess thionyl chloride. The residue was distilled under vacuum (air bath 100-110° C./˜10 mm) to provide the title compound, used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609669B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-ba22d4f86d254542b5d9526c68ae0697 |
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| Source note | uspto-grants-2013_12 |
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