HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86605428, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 11063219 | HCID 11063219 | — |
| Reactant | 3-[2,6-Dichloro-4-(3,3-dichloroallyloxy)-phenoxy]-propan-1-ol | HCID 11313980 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86605428 | HCID 86605428 | — |
Reaction Steps
0.39 ml of azodicarboxylic acid diisopropyl ester is added at 0° C. to 0.52 g of triphenylphosphine in 20 ml of tetrahydrofuran. After 30 minutes, 289 mg of 3-(4-hydroxyphenyl)cyclohexanone and 554 mg of 3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propan-1-ol in 10 ml of tetrahydrofuran are added dropwise thereto. After 24 hours at room temperature, the reaction mixture is concentrated and the residue is purified over silica gel. 3-(4-{3-[2,6-Dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-cyclohexanone is obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569727B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-4ee6432b6b8a41eb9978bfbecd4ca92d |
| Source note | uspto-grants-2009_08 |