HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cholesterol → HCID 69177522, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cholesterol | HCID 5997 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 5-Hexenoic Acid | HCID 15308 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69177522 | HCID 69177522 | 95% |
Reaction Steps
To a solution of cholesterol (2.0 g, 5.17 mM) in methylene chloride (20 mL) was added 5-hexenoic acid (0.68 mL, 5.69 mM) followed by the addition of DCC (1.60 g, 7.76 mM) and 4-PP (0.115 g, 0.78 mM) under nitrogen atmosphere. The resulting reaction mixture was stirred at ambient temperature for 1 h and worked up with the addition of methyl t-butyl ether (60 mL). The urea was filtered off, and the product was transferred to a separatory funnel, washed with 1N HCl (10 mL), water (30 mL) and brine (30 mL). The product was filtered after drying over MgSO4 and the solvent was evaporated to leave a residue. The product obtained in >95% yield was characterized by 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825166B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-ec786b6dfc2f40819e61d4398d76882e |
| Source note | uspto-grants-2004_11 |