反応 #1112346

反応方程式

2-bromoacetamide

DMF

cesium carbonate

methyl 4-hydroxy-2-methoxybenzoate

→

methyl 4-(2-amino-2-oxoethoxy)-2-methoxybenzoate

収率 91.4%

溶媒

DCM

反応条件

後処理

1. 1
   その他The tube was sealed
2. 2
   洗浄washed sequentially with 10 mL of 1M HCl, water, and brine
3. 3
   乾燥The solution was dried over sodium sulfate
4. 4
   ろ過filtered
5. 5
   その他the solvent removed

実験手順

To a sealed tube was added 2-bromoacetamide (2.272 g, 16.47 mmol), DMF (50 mL), cesium carbonate (7.15 g, 21.96 mmol) and methyl 4-hydroxy-2-methoxybenzoate (1.00 g, 5.49 mmol). The tube was sealed and heated for 16 hours at 85° C. The reaction mixture was diluted with DCM, washed sequentially with 10 mL of 1M HCl, water, and brine. The solution was dried over sodium sulfate, filtered and the solvent removed to give 1.2 grams of methyl 4-(2-amino-2-oxoethoxy)-2-methoxybenzoate (78% yield) as a yellow powder. The LC/MS data was obtained on a Shimadzu analytical LC/Micromass Platform LC (ESI+) at 220 nm using the following set of conditions: Waters Sunfire 5 μm C18, 4.6×30 mm column, with a gradient of 0-100% B (B=90% HPLC grade methanol/0.1% trifluoroacetic acid/10% HPLC grade water), (A=90% HPLC grade water/0.1% trifluoroacetic acid/10% HPLC grade methanol), in 2 minutes with a 1 minute hold at a rate of 4 mL/minute. 1H NMR (400 MHz, THF-d8) δ ppm 3.71-3.76 (m, 3 H), 3.80-3.84 (m, 3 H), 4.45 (s, 2 H), 6.56 (dd, J=8.66, 2.38 Hz, 1 H), 6.65 (d, J=2.26 Hz, 1 H), 6.77 (br. s., 1 H), 6.92 (br. s., 1 H), 7.75 (d, J=8.78 Hz, 2 H). LCMS Rt=1.385 min., m/z 240.2 (M+H), 92% purity.

出典