반응 #3163

ord-81a231be09734e50823c3b6abac323f1

반응 방정식

OCCOc1ccccc1O
2-(2-hydroxyethoxy)phenol
CCN(CC)CC
triethylamine
C1CCOC1
tetrahydrofuran
C=CC(=O)Cl
acryloyl chloride
C=CC(=O)Oc1ccccc1
reddish brown liquid
수율 62.0%
C=CC(=O)Oc1ccccc1
phenol acrylate
수율 62.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A 500-ml, two necked flask was equipped with magnetic stirring bar
  2. 2
    기타The triethylamine hydrochloride salt was removed by filtration
  3. 3
    기타the mother liquor was evaporated with a rotoevaporator
  4. 4
    workup.DISSOLUTIONThe remaining liquid was dissolved in chloroform
  5. 5
    세척washed with NaCl(aq.), NH4OH(10%), NaCl(aq.)
  6. 6
    건조dried over MgSO4
  7. 7
    기타The chloroform was removed with a rotoevaporator

실험 절차

A 500-ml, two necked flask was equipped with magnetic stirring bar, nitrogen atmosphere and an addition funnel. The flask was charged with 25 g of 2-(2-hydroxyethoxy)phenol (0.16 mol.), 33 g of triethylamine (0.32 mol.), 250 ml of tetrahydrofuran and 1 g of phenothiazine. Next, 30 g of acryloyl chloride (0.18 mol.) was slowly added to the reaction over 1 hour via the addition funnel. The triethylamine hydrochloride salt was removed by filtration and the mother liquor was evaporated with a rotoevaporator. The remaining liquid was dissolved in chloroform and washed with NaCl(aq.), NH4OH(10%), NaCl(aq.) and dried over MgSO4. The chloroform was removed with a rotoevaporator to yield 26 g (62%) of a reddish brown liquid. The product was confirmed by IR and 13C NMR.

출처

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