Ethyl Bromide → (5-Ethoxy-2-nitrophenyl)methanol

温度

50 °C

To a solution of 3-hydroxymethyl-4-nitro-phenol (510 mg, 3.0 mmol) in 5 mL of dry DMF was added bromoethane (540 mg, 5.0 mmol) and K2CO3 powder (500 mg). The resulting reaction mixture was warmed to 50° C. and stirred for 1 h. It was quenched by addition of 20 mL of H2O, extracted with diethyl ether (2×20 mL). The combined organic extracts were washed with brine (50 mL), dried (MgSO4), filtered, and concentrated in vacuo to afford (5-ethoxy-2-nitro-phenyl)-methanol as a pale yellow oil: 1H NMR (CDCl3, 500 MHz) δ 8.20 (d, 1H), 7.36 (s, 1H), 6.89 (m, 1H), 5.00 (s, 2H), 4.16 (q, 2H), 2.57 (br t, 1H), 1.49 (t, 3H).

1. customThe resulting reaction mixture
2. customIt was quenched by addition of 20 mL of H2O
3. extractionextracted with diethyl ether (2×20 mL)
4. washThe combined organic extracts were washed with brine (50 mL)
5. dry with materialdried (MgSO4)
6. filtrationfiltered
7. concentrationconcentrated in vacuo

ORDレコード

ord-4ab8845c5a1b403aada72f8e1412ef9b

出典データセット

uspto-grants-2008_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07465730B2