HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (R)-Phenyl(p-tolyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Reactant | HCID 178420449 | HCID 178420449 | — |
| Product | (R)-Phenyl(p-tolyl)methanol | HCID 7003729 | — |
Reaction Steps
An operation was carried out in the same manner as in Example 1, except that 0.40 mL (0.40 mmol) of an anhydrous THF solution (1.0 mol/L) of phenylmagnesium bromide was used instead of the anhydrous 1,4-dioxane solution of diphenylmagnesium. Thus, (R)-4-methylbenzhydrol was obtained. The conversion rate of the raw material was 98%, while the enantiomeric excess was 39% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563786B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-b06b146eaa6f4ae1b3da036c8094e0b9 |
| Source note | uspto-grants-2013_10 |