HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium borohydride → HCID 70509211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium borohydride | HCID 169536 | — |
| Reactant | HCID 70507886 | HCID 70507886 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70509211 | HCID 70509211 | — |
Reaction Steps
According to the procedures detailed in Example 3, benzhydryl 2-methyl-1-oxo-6-(2-phenoxyacetamido)carbapenam-3-carboxylate (138 mg., 0.28 mmole) in 15 ml. of methylene chloride was reduced with tetrabutylammonium borohydride (18 mg., 0.07 mmole) at -78° C., monitored and isolated as a washed, dried methylene chloride solution of benzhydryl 1-hydroxy-2-methyl-6-(2-phenoxyacetamido)carbapenam-3-carboxylate [Rf 0.24 (4:1 chloroform:ethyl acetate)]. If desired, the product is further isolated by evaporation to dryness in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04429128 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-073a15dbf3cc457386bb68c623f16951 |
| Source note | uspto-grants-1984_01 |