HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 86738085, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 7203539 | HCID 7203539 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86738085 | HCID 86738085 | — |
Reaction Steps
3α-Acetoxy-5β-cholanic acid (4.18 g; 10 mmoles) was added to 60 ml of anhydrous benzene. The solution was cooled with ice, and with stirring, 4.5 ml of thionyl chloride was gradually added dropwise. After the addition, the mixture was reacted at room temperature for 2.5 hours with stirring. The reaction mixture was concentrated under reduced pressure, and 20 ml of anhydrous benzene was added to the residue. The mixture was repeatedly concentrated under reduced pressure to remove the thionyl chloride contained in the residue. The resulting solid crude product, 3α-acetoxy-5β-cholanyl chloride, was used as a starting compound in the subsequent step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04298537 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-9914184968be41d6bfd97753ac1df6d0 |
| Source note | uspto-grants-1981_11 |