HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → HCID 131732618, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Ruthenium | HCID 23950 | — |
| Reactant | 1-Phenylethanol, (S)- | HCID 443135 | — |
| Reactant | HCID 131732619 | HCID 131732619 | — |
| Solvent | Triethylammonium formate | HCID 11084032 | — |
| Product | HCID 131732618 | HCID 131732618 | — |
Reaction Steps
In a 25-ml Schlenk tube, 4.9 mg (0.00339 mmol, S/C=1000) of the ruthenium dimer complex produced in Example 5, acetophenone (0.82 g, 6.86 mmol), and 3.4 ml of a formic acid-triethylamine (5:2) azeotrope were mixed with each other, and the reaction was allowed to proceed at 60° C. for 5 hours. GC analysis of the reaction liquid showed that (S)-1-phenylethanol was formed with a conversion of 98.9% and 96.6% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987492B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-98611643134143cea3d7df99fa8ee6f8 |
| Source note | uspto-grants-2015_03 |