HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 131717630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 131717631 | HCID 131717631 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131717630 | HCID 131717630 | — |
Reaction Steps
(1S,5S,6S,7R)-3-[4-Methoxycarbonyl-1(EZ)-butenyl]-6-[4(RS)-fluoro-3-oxo-(E )-1-octenyl]-7-tetrahydropyranyloxybicyclo[3.3.0]oct-2-ene bicyclo[3.3.0]oct-2-ene (5) (0.088g) was dissolved in methanol. Into the solution, sodium borohydride (0.008 g) was added at 0° C. and the mixture was stirred for 30 minutes. The reaction mixture was treated by a usual manner to give (1S,5S,6S,7R)-3-[4-methoxycarbonyl-1(EZ)-butenyl]-6-[4(RS)-fluoro-3(R S)-hydroxy-(E)-1-octenyl]-7-tetrahydropyranyloxybicyclo[3.3.0]oct-2-ene (5") as a colorless oily product. Yield: 0.089 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162370 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-faaeaad4fd744863ac05942bca211fa3 |
| Source note | uspto-grants-1992_11 |