反応 #566329

ord-8e53511544cd42e3a3d05a2fbba82823

反応方程式

C=CCCO
3-buten-1-ol
[H-].[Na+]
NaH
O=C(O)CBr
bromo-acetic acid
C=CCCOCC(=O)O
title compound
収率 126.8%
C=CCCOCC(=O)O
But-3-enyloxy-acetic acid
収率 126.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas then added
  2. 2
    workup.WAITthe mixture kept for additional 5 min. at 0° and for 2 h at ambient temperature
  3. 3
    workup.ADDITIONPouring
  4. 4
    抽出ice/HCl dil., twofold extraction with AcOEt
  5. 5
    洗浄washing with brine
  6. 6
    乾燥drying over natrium sulfate and evaporation of the solvents

実験手順

To 480 mg of NaH (50% in mineral oil, ˜20 mmol) in 10 ml of abs. THF was added at 0° 721 mg of 3-buten-1-ol (10 mmol) and the mixture stirred for 5 min. (H2-evolution). 1.39 g of bromo-acetic acid (10 mmol), dissolved in 10 ml of THF, was then added and the mixture kept for additional 5 min. at 0° and for 2 h at ambient temperature. Pouring onto crashed ice/HCl dil., twofold extraction with AcOEt, washing with brine, drying over natrium sulfate and evaporation of the solvents afforded 1.65 g of the title compound, contaminated with mineral oil, but sufficiently pure for the next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06642389B2uspto-grants-2003_11