HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Difluorobenzaldehyde → alpha-Cyclopropyl-2,4-difluorobenZenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | 4-Chloro-alpha-cyclopropylbenzenemethanol | HCID 86679 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | alpha-Cyclopropyl-2,4-difluorobenZenemethanol | HCID 58392431 | — |
Reaction Steps
The title compound was prepared starting from 1.50 g (10.55 mmol) of 2,4-difluorobenzaldehyde and 31.7 ml (15.83 mmol) of a 0.5N solution of cyclopropylmagnesium bromide in tetrahydrofuran in analogy to the synthesis of the compound from Example 153A. 0.33 g (17% of theory) of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063234B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-99130d1df02c4b409288b4f8ab6ed2e5 |
| Source note | uspto-grants-2011_11 |