반응 #57985

ord-fcdd33fd173d441c8d602b558d83885f

반응 방정식

CC(C)OC(=O)N=NC(=O)OC(C)C
Diisopropyl azodicarboxylate
COC(=O)c1cc2cc(O)ccc2o1
5-hydroxybenzofuran-2-carboxylic acid methyl ester
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
OCCN1CCCC1
1-(2-hydroxyethyl)-pyrrolidine
COC(=O)c1cc2cc(OCCN3CCCC3)ccc2o1
5-(2-pyrrolidin-1-yl-ethoxy)benzofuran-2-carboxylic acid methyl ester
수율 58.2%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the solvent was removed
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in a 2:1 mixture of Et2O
  3. 3
    세척The solution was washed with 1.0M aqueous NaOH
  4. 4
    추출The product was extracted into 1.0 M hydrochloric acid
  5. 5
    세척the combined acid extracts were washed with Et2O
  6. 6
    온도The extracts were cooled
  7. 7
    추출The basic solution was extracted with CH2Cl2
  8. 8
    건조the organic layer was dried over anhydrous MgSO4
  9. 9
    농축concentrated

실험 절차

Anhydrous tetrahydrofuran (15 ml) was added to a mixture of 5-hydroxybenzofuran-2-carboxylic acid methyl ester (1.10 g, 5.7 mmol), triphenylphosphine (1.50 g, 5.7 mmol), and 1-(2-hydroxyethyl)-pyrrolidine (0.66 g, 5.7 mmol) under a nitrogen atmosphere. Diisopropyl azodicarboxylate (1.15 ml, 5.8 mmol) was slowly added to the solution at room temperature. After 2 days, the solvent was removed and the residue was dissolved in a 2:1 mixture of Et2O:EtOAc (150 ml). The solution was washed with 1.0M aqueous NaOH. The product was extracted into 1.0 M hydrochloric acid and the combined acid extracts were washed with Et2O. The extracts were cooled and the pH of the extracts was adjusted to pH 12 with 50% aqueous NaOH. The basic solution was extracted with CH2Cl2 and the organic layer was dried over anhydrous MgSO4, and concentrated to give 5-(2-pyrrolidin-1-yl-ethoxy)benzofuran-2-carboxylic acid methyl ester (0.96 g) as an amber colored solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07420089B2uspto-grants-2008_09