Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5beta-Cholan-24-oic acid | HCID 92803 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54351697 | HCID 54351697 | — |
Reaction Steps
A mixture of 0.5 g (1.39 mmol) of 5β-cholanic acid (Aldrich), 0.4 mL (4.6 mmol) of oxalyl chloride, and 10 mL of methylene chloride was heated in a sealed reaction vessel at 60° C. for 15 minutes. The volatiles were distilled off to give 5β-cholanoyl chloride as a colorless solid in quantitative yield. m.p. 104-106° C. 1H NMR (CDCl3, 500 MHz): δ 2.94 (m, 1H), 2.83 (m, 1H), 2.00-0.67 (m, 37H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580384B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-500083ab6a344a1997446d8df4951bd9 |
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| Source note | uspto-grants-2013_11 |
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