反应 #1328398

ord-e89b292ed1244b179693e2025c7e0f47

反应方程式

O=C([O-])CCCCCBr
6-bromohexanoate
CO
methanol
COC(=O)CCCCCBr
product ( 1 )
收率 93.0%
COC(=O)CCCCCBr
Methyl 6-bromohexanoate
收率 93.0%

试剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他was bubbled hydrogen chloride gas for 1–2 minutes
  2. 2
    浓缩concentrated via rotary evaporation
  3. 3
    workup.ADDITIONThe residue was diluted with 500 mL of diethyl ether
  4. 4
    洗涤washed with 150 mL of de-ionized water, 200 mL of saturated sodium bicarbonate
  5. 5
    干燥The organic phase was dried over anhydrous magnesium sulfate
  6. 6
    过滤filtered
  7. 7
    浓缩concentrated via rotary evaporation
  8. 8
    workup.DISTILLATIONThe residue was distilled under vacuum

实验过程

To a 2 liter round bottom flask, charge with 99.7 g (0.511 mol) of 6-bromohexanoate (Aldrich Chemical Co., Milwaukee, Wis.) and 1 liter of methanol, was bubbled hydrogen chloride gas for 1–2 minutes. The mixture was stirred at 20–30° C. for 18 h and then concentrated via rotary evaporation. The residue was diluted with 500 mL of diethyl ether and washed with 150 mL of de-ionized water, 200 mL of saturated sodium bicarbonate, and then once again with 200 mL of de-ionized water. The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated via rotary evaporation. The residue was distilled under vacuum to afford 99.6 g of the product (1) as a colorless oil (93%): b.p.=93–96° C. at 3 mm Hg: 1H NMR (d6-DMSO) d 3.57 (3H, s), 3.51 (2H, t), 2.30 (2H, t), 1.78 (2H, pentet) and 1.62–1.28 (4H, m) ppm.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07115248B2uspto-grants-2006_10