HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroacetonitrile → p-Chloro-alpha,alpha-dimethylbenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | p-Chloro-alpha,alpha-dimethylbenzyl alcohol | HCID 74808 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | p-Chloro-alpha,alpha-dimethylbenzyl alcohol | HCID 74808 | — |
| Product | HCID 66918649 | HCID 66918649 | — |
Reaction Steps
To a suspension of sodium hydride (5.63 mg, 0.117 mmol) in ether was added a solution of 2-(4-chloro-phenyl)-propan-2-ol (CAS 1989-25-9) in ether (1.5 ml) at 0° C. The mixture was stirred for 90 minutes, then trichloroacetonitrile (112 μl, 1.11 mmol) was added and stirring was continued for 3 h at 0° C. Then all volatiles were removed and pentane (1 ml) and MeOH (4.74 μl) were added. The suspension was stirred for 1 h. Filtration and concentration of the filtrate yielded the title compound in a mixture with 2-(4-chloro-phenyl)-propan-2-ol which was used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893099B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-cd42fc80f07449b2ba6e827e833976b4 |
| Source note | uspto-grants-2011_02 |