HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 13839173, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Bromovaleryl chloride | HCID 521173 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13839173 | HCID 13839173 | — |
Reaction Steps
In a typical run, 2.6 equivalents of phenyl magnesium bromide are added to 1.0 equivalent of 5-bromopentanoyl chloride dissolved in dried diethyl ether under inert atmosphere at 0° C. and stirred during 15 minutes. After this time the mixture is warmed up to room temperature, and then ammonium chloride is added slowly to the mixture, and worked up in the usual manner to produce 5-bromo-1,1-diphenyl-1-pentanol as a white solid. The crude product is then refluxed during 6 hours with p-toluenesulfonic acid (ratio 60:1) under benzene, and worked up in the usual manner to yield 5-bromo-1,1-diphenyl-1-pentene as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145352B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-4bb2e62804a74ba8b5cd6ecd9501f413 |
| Source note | uspto-grants-2015_09 |