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Ethyl 3-(3-aMinophenyl)acrylate synthesis

7synthesis methods
-

Yield:58186-45-1 100%

Reaction Conditions:

with stannous chloride in methanol at 65; for 2 h;

Steps:

2 Step 2: (£)-Methyl 3-(3-aminophenyl)acrylate

Step 2: (£)-Methyl 3-(3-aminophenyl)acrylate [00393] A suspension of (£)-methyl 3-(3-nitrophenyl)acrylate (1.95 g, 9.40 mmol), tin (II) chloride dihydrate (7.20 g, 31.9 mmol), and methanol (27 mL) was heated at 65 °C for 2 h, cooled to room temperature, and poured into ice water (100 mL). The reaction mixture was diluted with saturated NaHC03 (200 mL) and extracted with ethyl acetate (3 x400 mL). The organic extracts were washed (200 mL brine), dried (Na2S04), and concentrated under reduced pressure to give (£)-methyl 3-(3-aminophenyl)acrylate (1.68 g, 100%) as yellow solid. 1H MR (400 MHz, DMSO-i): δ 7.48 (d, J= 15.8 Hz, 1H), 7.06 (t, J= 7.8 Hz, 1H), 6.85-6.79 (m, 2H), 6.65-6.61 (m, 1H), 6.41 (d, J= 15.8 Hz, 1H), 5.19 (s, 2H), 3.71 (s, 3H).

References:

WO2017/49172,2017,A1 Location in patent:Paragraph 00393