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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Reactant | Sodium Perborate | HCID 517072 | — |
| Reactant | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| Reactant | Methyl 3-ethenyl-1-naphthalenecarboxylate | HCID 66896260 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-(2-hydroxyethyl)-1-naphthalenecarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889714B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-30d7d51b3abb4712842c35291ed1d6c0 |
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| Source note | uspto-grants-2014_11 |
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