HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 53837977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13341408 | HCID 13341408 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 53837977 | HCID 53837977 | — |
Reaction Steps
200 mg of 1α,3β,24trihydroxycholesta-5,7-diene prepared and separated in the same way as in Example 14, (D-1) was reacted with 2ml. of acetic anhydride and 5 ml. of pyridine at 95° C. for 3 hours. The reaction mixture was placed in ice water, and extracted with 40 ml. of diethyl ether. The ethereal phase was washed with dilute hydrochloric acid, then with alkali, and further with water, and dried. The ether was evaporated off to afford 1α,3β,24-triacetoxycholesta-5,7-diene as a slightly yellowish oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022891 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-3379a3408a0a49509eeca4c1ba91e22d |
| Source note | uspto-grants-1977_05 |