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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154788Generated: November 1, 2026

Thionyl Chloride → HCID 86738085, compound

https://huagongshe.com/reaction/1154788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 7203539HCID 7203539—
SolventBenzeneHCID 241—
ProductHCID 86738085HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298537
Source datasetuspto-grants-1981_11
ORD IDord-9914184968be41d6bfd97753ac1df6d0
Source noteuspto-grants-1981_11