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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084565Generated: October 30, 2026

Triphenylphosphine → HCID 22733426, compound

https://huagongshe.com/reaction/2084565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2,2'-Dipyridyl disulfideHCID 65093—
ReactantDiisopropylethylamineHCID 81531—
Reactant(Tricyclo[3.3.1.1~3,7~]decan-2-ylidene)acetic acidHCID 2842562—
ReactantHCID 22733386HCID 22733386—
ReactantHCID 22733406HCID 22733406—
ReactantHCID 22733430HCID 22733430—
SolventDichloromethaneHCID 6344—
ProductHCID 22733426HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716865B1
Source datasetuspto-grants-2004_04
ORD IDord-45d29ac6cdaf45a9814c272cbec6f5c4
Source noteuspto-grants-2004_04