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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337599Generated: October 30, 2026

1,4-Bis(diphenylphosphino)butane → Methyl 3-(2-hydroxyethyl)-1-naphthalenecarboxylate

https://huagongshe.com/reaction/337599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
ReactantSodium PerborateHCID 517072—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
ReactantMethyl 3-ethenyl-1-naphthalenecarboxylateHCID 66896260—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(2-hydroxyethyl)-1-naphthalenecarboxylateHCID 66896170—

Reaction Steps

Methyl 3-ethenyl-1-naphthalenecarboxylate (1 eq.) from the previous step, [Ir(COD)Cl]2 (0.025 eq.) and DPPB (0.05 eq.) were combined in THF (0.12 M). To this solution was then added 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.2 eq.) and the resulting red solution was stirred at RT for 16 h. Finally, sodium perborate (0.1 M aqueous solution, 2 eq.) was added and the now black biphasic solution was vigorously stirred at RT for another 12 h. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were then washed further with 1 N aq. NaOH, water and brine. This was then dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford a pale yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→1:1 (v/v) EtOAc:Hex) afforded the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-30d7d51b3abb4712842c35291ed1d6c0
Source noteuspto-grants-2014_11