Diethyl 2-(4-methoxyphenyl)malonate → HCID 11355866、化合物

温度

40 °C

LiAlH4 (5.75 g, 0.15 mol) was suspended in ethyl ether (150 mL), and into this suspension solution compound 19 (16.85 g, 0.10 mol) dissolved in 50 ml ethyl ether was added dropwise. The resulting solution was stirred at 40° C. for 40 hr, and cooled in ice bath, and ethyl ether (15 ml) was introduced dropwise to destroy the excess LiAlH4 remaining in the solution. After the addition was completed, the resulting solution was added with 200 ml HCl aqueous solution (HCl/H2O, 1:2) and stirred for one hr. The organic phase was removed. The aqueous phase was extracted with ethyl ether (2×200 ml). The ether layer was combined with the collected organic phase, and then was washed with NaHCO3 aqueous solution (2%, 20 ml), water (20 ml), saturated sodium chloride solution (20 ml), dried, and filtered. The residual was recrystallized from benzene to yield 12 g (66%) product 20. 1 H-NMR (CDCl3, TMS, δ in ppm): 2.17 (s, 2H, --OH), 3.08 (m, 1H PhCH), 6.82 and 7.13 (q, 4 aromatic protons).

1. additionwas added dropwise
2. temperaturecooled in ice bath
3. customto destroy the excess LiAlH4 remaining in the solution
4. additionAfter the addition
5. additionthe resulting solution was added with 200 ml HCl aqueous solution (HCl/H2O, 1:2)
6. stirringstirred for one hr
7. customThe organic phase was removed
8. extractionThe aqueous phase was extracted with ethyl ether (2×200 ml)
9. washwas washed with NaHCO3 aqueous solution (2%, 20 ml), water (20 ml), saturated sodium chloride solution (20 ml)
10. customdried
11. filtrationfiltered
12. customThe residual was recrystallized from benzene

ORDレコード

ord-6f9d352c9cae4323a0f44ef86517cab5

出典データセット

uspto-grants-1992_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05091274