HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Chlorophenyl)ethanone → Benzenemethanol, 3-chloro-.alpha.,.alpha.-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Chlorophenyl)ethanone | HCID 14933 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzenemethanol, 3-chloro-.alpha.,.alpha.-dimethyl- | HCID 593110 | 93.6% |
Reaction Steps
Methylmagnesium bromide (3.6 mL, 10.67 mmol, Aldrich, 3 M solution in ether) was added to a cooled (−10° C.) solution of 3-chloroacetophenone (1.5 g, 9.7 mmol) in anhydrous ether slowly over 30 min. After complete addition, the reaction mixture was slowly warmed to room temperature, stirred for 18 hours. Again cooled (−5° C.), than quenched with sat. ammonium chloride solution over 30 min. The reaction mixture was extracted with ether, dried, filtered and concentrated to afford 1.55 g of 2-(3-chlorophenyl)propan-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888366B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-908307a7f4c64e7bb57029ee691457c9 |
| Source note | uspto-grants-2011_02 |