HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70591639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70589714 | HCID 70589714 | — |
| Product | HCID 70591639 | HCID 70591639 | — |
Reaction Steps
0.1 g. 11-hydroxy-15,15-ethylenedioxy-9-oxo-13-thia-5-prostenoic acid is reduced with NaBH4 analogously to Example 14 and the 9,11-dihydroxy-15,15-ethylenedioxy-13-thia-5-prostenoic acid obtained subsequently stirred at room temperature for 2 hours with 10 ml. IN aqueous HCl and 10 ml. dioxan. The reaction mixture is saturated with NaCl extracted with benzene, the organic phase dried and the solvent distilled off to obtain, as the residue, 9,11-dihydroxy-15-oxo-13-thia-5-prostenoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04080458 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-acddb03abf8445a994d36315118cd1ce |
| Source note | uspto-grants-1978_03 |