반응 #3168

ord-77519deec78d44d89cdc131b10b54df8

반응 방정식

C=CC(=O)Cl
acryloyl chloride
O=C1NCC(CO)O1
5-hydroxymethyl-oxazolidin-2-one
CCN(CC)CC
triethylamine
c1ccc2c(c1)Nc1ccccc1S2
phenothiazine
C=CC(=O)OCC1CNC(=O)O1
5-Acryloyloxymethyl-oxazolidin-2-one

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타round bottomed flask equipped with a paddle stirrer
  2. 2
    workup.ADDITIONwere added dropwise in such a way that the contents of the flask
  3. 3
    온도were maintained at 30° C. or less
  4. 4
    workup.ADDITIONWhen the addition
  5. 5
    workup.STIRRINGthe contents were stirred overnight at room temperature
  6. 6
    여과The triethylamine hydrochloride was filtered
  7. 7
    여과The solution was filtered
  8. 8
    농축The solution was concentrated
  9. 9
    기타by purging with a stream of air
  10. 10
    workup.ADDITIONa mixture of the desired product

실험 절차

105 g (0.90 mol.) of 5-hydroxymethyl-oxazolidin-2-one were placed into a one liter, three necked, round bottomed flask equipped with a paddle stirrer and thermometer. This was followed by 500 ml of tetrahydrofuran, 101 g (1.0 mol.) of triethylamine and 0.5 g of phenothiazine. Stirring was started as 90 g (1.0 mol.) of acryloyl chloride were added dropwise in such a way that the contents of the flask were maintained at 30° C. or less. When the addition was complete, the contents were stirred overnight at room temperature. The triethylamine hydrochloride was filtered and the solution was allowed to stand over NaHCO3 and Na2SO4. The solution was filtered, transferred to a one liter, round bottomed flask and placed on a rotoevaporator. The solution was concentrated by purging with a stream of air while rotating the flask. The resulting liquid was confirmed by 13C NMR to contain a mixture of the desired product and unreacted starting material.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733648uspto-grants-1998_03