反应 #9038

ord-d3bccefe8a7947608797d443fe4904be

反应方程式

COS(=O)(=O)OC
dimethyl sulfate
CCOC(=O)c1c(C)cccc1O
ethyl 6-methylsalicylate
O.[Li+].[OH-]
lithium hydroxide monohydrate
CCOC(=O)c1c(C)cccc1OC
ethyl 2-methoxy-6-methylbenzoate
收率 91.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to reflux for 1 hour
  2. 2
    洗涤washed with saturated aqueous NaHCO3 (4×10 mL)
  3. 3
    干燥dried (MgSO4)
  4. 4
    浓缩concentrated
  5. 5
    其他Purification of the crude material by column chromatography on silica gel (9:1 hexanes-EtOAc)

实验过程

To a solution of ethyl 6-methylsalicylate (1.27 g, 6.97 mmol) in THF (35 mL) was added lithium hydroxide monohydrate (0.594 g, 14.2 mmol) followed by dimethyl sulfate (1.00 mL, 10.6 mmol). The resultant mixture was heated to reflux for 1 hour then cooled to room temperature. The mixture was diluted with diethyl ether (70 mL), washed with saturated aqueous NaHCO3 (4×10 mL), dried (MgSO4) and concentrated. Purification of the crude material by column chromatography on silica gel (9:1 hexanes-EtOAc) provided 1.23 g (91%) of ethyl 2-methoxy-6-methylbenzoate as a white solid. 1H NMR (CDCl3) δ 1.38 (t, 3H, J=7.2 Hz), 2.30 (s, 3H), 3.82 (s, 3H), 4.40 (q, 2H, J=7.2 Hz), 6.76 (d, 1H, J=8.4 Hz), 6.79 (d, 1H, J=7.8 Hz), 7.23 (dd, 1H, J=7.8, 8.4 Hz).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07091217B2uspto-grants-2006_08