4-Nitrobenzaldehyde → 4-Methyl-1-(4-nitrophenyl)pent-2-yne-1,4-diol

To a stirred −78° C. solution of 2-methylbut-3-yn-2-ol (6.1 mL, 63.5 mmol, 1.2 eq) in dry THF (250 mL), n-BuLi (62 mL, 2.3 M in hexane, 142 mmol, 2.7 eq) was added dropwise over 10 minutes under an inert atmosphere. After being stirred for 40 min at −78° C., a solution of 4-nitrobenz aldehyde (8 g, 52.9 mmol, 1 eq) in dry THF (50 mL) was added to the reaction mixture and stirring was continued for an additional 1 h at −78° C. The reaction mixture was then quenched with a saturated NH4Cl solution and extracted with EtOAc (2×200 mL). The combined organic layers were washed with water (200 mL) and brine (100 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue was purified by column chromatography (30% ethyl acetate in hexanes) to afford 4-methyl-1-(4-nitrophenyl)pent-2-yne-1,4-diol (8 g, 65%) as a yellow solid.

1. stirringstirring
2. waitwas continued for an additional 1 h at −78° C
3. customThe reaction mixture was then quenched with a saturated NH4Cl solution
4. extractionextracted with EtOAc (2×200 mL)
5. washThe combined organic layers were washed with water (200 mL) and brine (100 mL)
6. dry with materialdried over Na2SO4
7. filtrationfiltered
8. concentrationconcentrated in vacuo
9. customThe resulting residue was purified by column chromatography (30% ethyl acetate in hexanes)

ORD-Eintrag

ord-426bb18dba3e4c3b877f7eb54a1bb87d

Quelldatensatz

uspto-grants-2013_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08466148B2