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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863415Generated: October 26, 2026

Oxalyl chloride → 3beta-Acetoxy-5-cholenic acid chloride

https://huagongshe.com/reaction/863415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3beta-Acetoxy-5-cholenic acidHCID 11101791—
SolventDichloromethaneHCID 6344—
Product3beta-Acetoxy-5-cholenic acid chlorideHCID 12953337—

Reaction Steps

To a solution of 3β-acetoxy-5-cholenic acid (50.0 g, 118 mmole) in dry dichloromethane (200 ml) was added dropwise oxalyl chloride (30 ml, 448 mmole). The solution was stirred at room temperature for one hour and then concentrated in vacuo to obtain 3β-acetoxy-5-cholenic acid chloride 331. 1H NMR (400 MHz, CDCl3) δ: 0.70 (3H, s, 18--CH3), 0.95 (3H, d, 21--CH3), 1.05 (3H, s, 19--CH3), 2.04 (3H, s, --OCOCH3), 4.60 (1H, m, 3α-H), 5.38 (1H, m, 6-H). Compound 331 was used in the following step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721226
Source datasetuspto-grants-1998_02
ORD IDord-d5268be02a164516bad0cb3bf3d66993
Source noteuspto-grants-1998_02