HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethyl butanoate → 17alpha-Hydroxy-21-butanoyloxy-pregna-4,9(11)-diene-3,20-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethyl butanoate | HCID 193290 | — |
| Reactant | Anecortave | HCID 7074810 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 17alpha-Hydroxy-21-butanoyloxy-pregna-4,9(11)-diene-3,20-dione | HCID 86720232 | — |
Reaction Steps
A mixture of 1 g (2.879 mM) of 17α,21-dihydroxy-pregna-4,9(11)-diene-3,20-dione and 10 ml of trifluoroethyl butanoate in 100 ml of acetone was reacted at 45° C. in the presence of 5 g of Candida cylindracea lipase for 8-10 hours, adding 1 g of lipase at regular time intervals. After completion of the reaction, the lipase was filtered off and the filtrate was concentrated under vacuum, taking up the residue three times with acetone. The semi-solid residue was purified by chromatography on a silica gel column with a dichloromethane/methanol 99:1 mixture. The less polar components were removed, to obtain the richer fraction which was evaporated to yield 0.95 g (2.29 mM) of 17α-hydroxy-21-butanoyloxy-pregna-4,9(11)-diene-3,20-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865690B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-b02d7551d0684fd2b2feceb34728a024 |
| Source note | uspto-grants-2014_10 |