Toluene → Methyl 16-bromohexadecanoate
反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18].[C:20]1(C)C=CC=CC=1.COC(OC)OC>CO>[CH3:20][O:18][C:17](=[O:19])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][Br:1]参加物
反応条件
- 温度
- 55 °C
実験手順
16-Bromo-hexadecanoic acid (6.0 g) was dissolved in MeOH (35 mL), toluene (100 mL) and trimethylorthoformate (20 mL), then Amberlyst 15 from Fluka (1.4 g) was added. The mixture was stirred at 55° C. for 16 h. The mixture was evaporated to dryness and dried under vacuum for 16 h to yield 7.7 g. The residue was suspended in MeOH (ca. 50 mL) and stirred for ca ½ h. The amberlyst 15 was filtered off after stirring with DCM (30 mL) for ½ h. The filtrate was concentrated to remove the DCM, and the clear solution was cooled and more MeOH (ca 20 mL, total ca 40 mL) was added. The flask was cooled and more crystals precipitated and after stirring for 30 min, the crystals were filtered off and washed with cold MeOH. The white crystals were dried under vacuum to yield 5.61 g.
後処理
- customThe mixture was evaporated to dryness
- customdried under vacuum for 16 h
- customto yield 7.7 g
- stirringstirred for ca ½ h
- filtrationThe amberlyst 15 was filtered off
- stirringafter stirring with DCM (30 mL) for ½ h
- concentrationThe filtrate was concentrated
- customto remove the DCM
- temperaturethe clear solution was cooled
- additionmore MeOH (ca 20 mL, total ca 40 mL) was added
- temperatureThe flask was cooled
- custommore crystals precipitated
- stirringafter stirring for 30 min
- filtrationthe crystals were filtered off
- washwashed with cold MeOH
- customThe white crystals were dried under vacuum
- customto yield 5.61 g
出典と根拠
- ORDレコード
- ord-aab525d342c445429b87628c37e56b6d
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08648041B2
反応ノート
読み込み中…