HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86605427, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-[2,6-Dichloro-4-(3,3-dichloroallyloxy)-phenoxy]-propan-1-ol | HCID 11313980 | — |
| Reactant | HCID 68856340 | HCID 68856340 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86605427 | HCID 86605427 | — |
Reaction Steps
0.93 ml of azodicarboxylic acid diisopropyl ester is added at 0° C. to 1.26 g of triphenylphosphine in 30 ml of tetrahydrofuran and stirring is carried out for 30 minutes. 0.76 g of 3-(4-hydroxybenzoyl)isoxazole and 1.38 g of 3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propan-1-ol in 10 ml of tetrahydrofuran are then added dropwise and stirring is carried out at room temperature for 24 hours. After the reaction mixture has been concentrated and purified over silica gel, (4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-phenyl)-isoxazol-3-yl-methanone 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-c320c3f6c9584494ae38cfb7b082ed37 |
| Source note | uspto-grants-2009_08 |