HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 69652268, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Dichlorophenethyl alcohol | HCID 2734099 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | Methyl 3-hydroxy-4-iodobenzoate | HCID 10378812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69652268 | HCID 69652268 | — |
Reaction Steps
6.6 g of triphenylphosphine and 5 g of 4-Iodo-3-hydroxy-benzoic acid methyl ester were dissolved in 65 ml of anhydrous THF. The solution was cooled to 0 ° C. to 10° C. and a solution of 3.7 ml DEAD in 7.5 ml anhydrous THF was added dropwise over 20 min. The reaction was warmed to RT and stirred for 45 min. A solution of 2.8 ml 2-(2,4-Dichlorophenyl)-ethanol in 3 ml anhydrous THF was added with cooling. The reaction was stirred at RT for 3 h, then the solvents were removed under reduced pressure. The residue was treated with n-heptane:ethyl acetate 1:1. The filtrate was dried under reduced pressure. The product was purified by silica gel chromatography, eluting with n-heptane:ethyl acetate/4:1 to n-heptane:ethyl acetate/1:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953857B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-29c9c43d9a344ce6980be6767fe10806 |
| Source note | uspto-grants-2005_10 |