HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 22733426, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,2'-Dipyridyl disulfide | HCID 65093 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (Tricyclo[3.3.1.1~3,7~]decan-2-ylidene)acetic acid | HCID 2842562 | — |
| Reactant | HCID 22733386 | HCID 22733386 | — |
| Reactant | HCID 22733406 | HCID 22733406 | — |
| Reactant | HCID 22733430 | HCID 22733430 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22733426 | HCID 22733426 | — |
Reaction Steps
2-(Adamantan-2-ylidene)-N-(2,4-dihydroxyphenyl)acetamide (formula VII) 3.0 g (adamantan-2-ylidene)acetic acid (formula R3COOH), 5.91 g triphenylphosphane and 4.95 g dipyridyldisulfide, dissolved in 100 ml of dichloromethane, are stirred at room temperature overnight. To the mixture obtained, 5.13 ml of N-ethyl-diisopropylamine and 4.83 g 2,4-dihydroxyaniline hydroxide (formula V) are added and the mixture is stirred for about 24 hours, the solvent is evaporated off, the evaporation residue is dissolved in ethyl acetate and extracted with a saturated aqueous NaH2PO4 solution and brine. The organic layer is dried, the solvent is evaporated off and the residue is purified by chromatography. The title compound is obtained (m.p. 166-169°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06716865B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-45d29ac6cdaf45a9814c272cbec6f5c4 |
| Source note | uspto-grants-2004_04 |