反応 #2487416

ord-3e0a866ac84246e2a9186cf5236c4666

反応方程式

COc1ccc(O)cc1
Hydroquinone monomethyl ether
CC(Br)C(=O)Br
2-Bromopropionyl bromide
C=C(C)C(=O)OCCO
2-hydroxyethyl methacrylate
CCN(CC)CC
triethylamine
C=C(C)C(=O)OCCOC(=O)C(C)Br
oil
収率 63.9%
C=C(C)C(=O)OCCOC(=O)C(C)Br
2-((2-bromopropanoyl)oxy)ethyl methacrylate
収率 63.9%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過filtered
  2. 2
    workup.ADDITIONfurther treated with more MEHQ (˜15 mg)
  3. 3
    その他evaporated to dryness

実験手順

2-Bromopropionyl bromide (18 g, 0.083 mol, 1 m.e) in ethyl acetate (30 mL) was added dropwise to a mixture of 2-hydroxyethyl methacrylate (HEMA) (16.26 g, 0.125 mol, 1.5 m.e) and triethylamine (9.26 g, 0.091 mol, 1.1 m.e) in ethyl acetate (80 mL) at 0° C. under a N2 environment. Hydroquinone monomethyl ether (MEHQ) was added as an inhibitor at this stage (−15 mg, 1.2×10−4 mol). The reaction mixture was stirred overnight, then filtered, further treated with more MEHQ (˜15 mg) and then evaporated to dryness to give a clear colourless oil (14 g, 0.053 mol, 63% yield). 1H NMR (200 MHz, CDCl3) δ 1.82 (d, J=8 Hz, 3H, CH3CH—), 1.95 (s, 3H, (CH3CCO—), 4.36-4.46 (m, 5H, 2× —CH2O— and —CHBr), 5.60 (br. s, 1H, vinyl), 6.13 (s, 1H, vinyl) ppm.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08795782B2uspto-grants-2014_08