반응 #80269

ord-2d529106f10b41eca09d69b8dda1347e

반응 방정식

O=C(Cl)Oc1ccccc1
phenylchloroformate
CN(C)CCO
N,N-dimethylethanolamine
CCN(CC)CC
triethylamine
CN(C)CCOC(=O)Oc1ccccc1
8
CN(C)CCOC(=O)Oc1ccccc1
N-[2-((Phenoxycarbonyl)oxy)ethyl]-N,N-dimethylamine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 500 ml three-necked round-bottomed flask equipped with an internal thermometer
  2. 2
    온도reflux
  3. 3
    workup.ADDITIONcondenser, mechanical stirrer, addition funnel, and argon inlet
  4. 4
    workup.ADDITIONAfter addition
  5. 5
    온도the mixture is heated
  6. 6
    온도to reflux for 3 h
  7. 7
    세척The cooled mixture is washed with saturated sodium bicarbonate solution (2×100 ml) and water (100 ml)
  8. 8
    건조The organic phase is dried over MgSO4
  9. 9
    여과filtered
  10. 10
    농축concentrated first by rotary evaporation at 50° C. (water aspirator vacuum)

실험 절차

To a 500 ml three-necked round-bottomed flask equipped with an internal thermometer, reflux condenser, mechanical stirrer, addition funnel, and argon inlet are added N,N-dimethylethanolamine (25.00 g, 0.281 mol), toluene (200 ml), and triethylamine (31.21 g, 0.309 mol). The mixture is treated with a solution of phenylchloroformate (43.91 g, 0.281 mol) dissolved in 50 ml of toluene over 15 min. After addition is complete, the mixture is heated to reflux for 3 h. The cooled mixture is washed with saturated sodium bicarbonate solution (2×100 ml) and water (100 ml). The organic phase is dried over MgSO4, filtered, and concentrated first by rotary evaporation at 50° C. (water aspirator vacuum) and then at 60° C. (0.05 mmHg) in a Kugelrohr oven to give 8 as a light yellow oil, 49.93 g (85%) that crystallizes on standing.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05616546uspto-grants-1997_04