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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168575Generated: October 30, 2026

Sodium Hydroxide → HCID 178436370, compound

https://huagongshe.com/reaction/2168575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-VinylbenzylamineHCID 11073466—
ReactantHCID 178446967HCID 178446967—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 178436370HCID 17843637062.3%

Reaction Steps

A solution of NaBH(OAc)3 (0.17 g, 0.8 mmol) and 4-vinylbenzylamine (0.26 g, 1.95 mmol) in 10 ml of dichloroethane is admixed dropwise at ambient temperature with a solution of 1,2-bis-(diphenylphosphino)-1′-diisopropylphosphino-4-(4-oxo-2-methylbut-2-yl)ferrocene (1.3 g, 1.2 mmol) in 5 ml of dichloroethane. The solution is held with stirring for 24 hours and then neutralized by addition of 1M aqueous sodium hydroxide solution. The aqueous phase is extracted with 2 times 30 ml of dichloromethane. The organic phases are combined, dried over MgSO4, and concentrated under reduced pressure. The crude product obtained is purified by chromatography on silica gel (CH2Cl2/MeOH, 95:5) to give 0.4 g (ρ=55%) of 1,1′,2-tris(diphenylphosphino)-2′-diisopropylphosphino-4-[2-methyl-5-(4-vinylbenzylamino)pent-2-yl]ferrocene in the form of a red-orange powder. The 31P NMR spectrum preserves, as expected, the A2B spin system appearance typical of these triphosphines, as described by Hierso et al. for the nonheterogeneizable analog in Org. Lett. 2004, 6, 3473-3476, with slightly modified chemical shifts.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045511B2
Source datasetuspto-grants-2015_06
ORD IDord-8962ad32bddd43c0b87e181ab13bf4ca
Source noteuspto-grants-2015_06