HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 131717632, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 131717633 | HCID 131717633 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131717632 | HCID 131717632 | — |
Reaction Steps
(1S,5S,6S,7R)-3-[4-Methoxycarbonyl-1(EZ)-butenyl]-6-[4,4-difluoro-3-oxo-(E )-1-octenyl]-7-tetrahydropyranyloxy-bicyclo[3.3.0]oct-2-ene (16) (0.196 g) was dissolved in methanol. To the solution, sodium borohydride (0.015 g) was added at 0° C., and the mixture was stirred for 30 minutes. After a usual work-up (1S,5S,6S,7R)-3-[4-methoxycarbonyl-1(EZ)-butenyl]-6-[4, 4-difluoro-3-(RS)hydroxy-(E)-1--octenyl]-7-tetrahydropyranyloxy-bicyclo[3.3.0]oct-2-ene (17) was obtained as a colorless oily product. Yield: 0.184 g (93%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162370 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-fbd596d58e4d4ebc91f37bfbbf5a543b |
| Source note | uspto-grants-1992_11 |